A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169446



Internal ID21313929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11676182..12174190hg38UCSC Ensembl
Outerchr9:11675235..12180135hg38UCSC Ensembl
Innerchr9:11676182..12174190hg19UCSC Ensembl
Outerchr9:11675235..12180135hg19UCSC Ensembl
Innerchr9:11666182..12164190hg18UCSC Ensembl
Outerchr9:11665235..12170135hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38504901
hg19504901
hg18504901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249105, nssv14251115, nssv14246109, nssv14241317, nssv14247563, nssv14241956, nssv14250387, nssv14247450, nssv14242402, nssv14244367, nssv14246948, nssv14241983, nssv14245859, nssv14242869, nssv14249244, nssv14244948, nssv14249439, nssv14248034, nssv14248554, nssv14242980, nssv14251010, nssv14241860, nssv14245803, nssv14250874, nssv14250959, nssv14246274, nssv14251252, nssv14243172
SamplesNGO_13, NGO_21, MLY_6, SNI_13, NGO_37, NGO_17, NGO_14, NGO_20, NGO_40, NGO_25, MLY_8, NGO_1, NGO_52, NGO_36, NGO_23, SNI_6, NGO_34, NGO_15, NGO_38
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169446
Frequency
Sample Size93
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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