A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005377



Internal ID19094594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3838382..3876759hg38UCSC Ensembl
Innerchr2:3885972..3924349hg19UCSC Ensembl
Innerchr2:3863847..3902224hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3838378
hg1938378
hg1838378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3703n100
Supporting Variantsnssv3571303
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)nsv1005377
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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