A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998391



Internal ID18811241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25256126..25302128hg38UCSC Ensembl
Innerchr1:25582617..25628619hg19UCSC Ensembl
Innerchr1:25455204..25501206hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3846003
hg1946003
hg1846003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv135n100
Supporting Variantsnssv3700863
Samples
Known GenesRHD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998391
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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