A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169751



Internal ID21313562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80566048..80588760hg38UCSC Ensembl
Outerchr6:80564619..80589336hg38UCSC Ensembl
Innerchr6:81275765..81298477hg19UCSC Ensembl
Outerchr6:81274336..81299053hg19UCSC Ensembl
Innerchr6:81332484..81355196hg18UCSC Ensembl
Outerchr6:81331055..81355772hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3824718
hg1924718
hg1824718
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250453, nssv14250654, nssv14249436, nssv14248011, nssv14243741, nssv14244896, nssv14250771, nssv14244459, nssv14248621, nssv14249188, nssv14240958, nssv14245180, nssv14243501, nssv14244243, nssv14243649, nssv14241140, nssv14245258, nssv14242332, nssv14246239, nssv14248819, nssv14247468
SamplesNGO_13, NGO_21, MLY_15, NGO_3, MLY_6, MLY_11, NGO_32, PML_1, MLY_13, NGO_31, PML_3, MLY_9, NGO_20, MLY_7, MLY_2, PML_4, NGO_16, NGO_55, NGO_42, MLY_10, NGO_15
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169751
Frequency
Sample Size93
Observed Gain1
Observed Loss20
Observed Complex0
Frequencyn/a


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