A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009931



Internal ID18752462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17100267..17161456hg38UCSC Ensembl
Innerchr1:17426762..17487951hg19UCSC Ensembl
Innerchr1:17299349..17360538hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3861190
hg1961190
hg1861190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3468895
Samples
Known GenesPADI2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009931
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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