A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997538



Internal ID19157074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:12076282..12102608hg38UCSC Ensembl
Innerchr2:12216408..12242734hg19UCSC Ensembl
Innerchr2:12133859..12160185hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3826327
hg1926327
hg1826327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726745
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)nsv997538
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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