A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009986



Internal ID19099205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:40877389..40909436hg38UCSC Ensembl
Innerchr1:41343061..41375108hg19UCSC Ensembl
Innerchr1:41115648..41147695hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3832048
hg1932048
hg1832048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv154n100
Supporting Variantsnssv3468951
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009986
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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