A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169646



Internal ID21313457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:18452078..18606845hg38UCSC Ensembl
Outerchr17:18416548..18626375hg38UCSC Ensembl
Innerchr17:18355392..18510158hg19UCSC Ensembl
Outerchr17:18319862..18529688hg19UCSC Ensembl
Innerchr17:18296117..18450883hg18UCSC Ensembl
Outerchr17:18260587..18470413hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38209828
hg19209827
hg18209827
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249877, nssv14250633, nssv14252001, nssv14246593, nssv14244648, nssv14250934, nssv14251567, nssv14243865, nssv14249394, nssv14242984, nssv14244486, nssv14241024, nssv14241658, nssv14246960, nssv14251071, nssv14252113, nssv14244991, nssv14250078, nssv14249728, nssv14242056, nssv14243333, nssv14250833, nssv14240766, nssv14244795, nssv14247168, nssv14243894, nssv14251344, nssv14250227, nssv14250983, nssv14249320, nssv14244863, nssv14244332, nssv14250072, nssv14246385, nssv14243444, nssv14247797, nssv14247900, nssv14241219, nssv14245789, nssv14244552, nssv14250754, nssv14244008
SamplesNGO_21, MLY_15, SNI_2, MLY_6, MLY_5, NGO_27, SNI_13, SNI_8, MLY_11, MLY_17, NGO_28, MLY_12, SNI_10, NGO_10, NGO_46, NGO_4, MLY_13, NGO_43, MLY_16, PML_3, NGO_50, NGO_30, MLY_9, NGO_20, NGO_47, PML_4, NGO_16, NGO_1, NGO_52, NGO_55, NGO_23, SNI_5, SNI_6, NGO_42, NGO_5, NGO_8, NGO_44, MLY_4, NGO_11, NGO_51, SNI_4
Known GenesCCDC144B, FAM106A, KRT16P1, LGALS9C, LOC339240, USP32P2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169646
Frequency
Sample Size93
Observed Gain17
Observed Loss24
Observed Complex0
Frequencyn/a


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