A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3577252



Internal ID18875533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:62131272..62177288hg38UCSC Ensembl
Innerchr2:62358407..62404423hg19UCSC Ensembl
Innerchr2:62211911..62257927hg18UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3846017
hg1946017
hg1846017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010519
Supporting Variants
Samples
Known GenesCOMMD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3577252
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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