A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008437



Internal ID19097655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14871921..14924450hg38UCSC Ensembl
Innerchr2:15012045..15064574hg19UCSC Ensembl
Innerchr2:14929496..14982025hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3852530
hg1952530
hg1852530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3729n100
Supporting Variantsnssv3577110, nssv3577109
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)nsv1008437
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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