A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003959



Internal ID19093176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:62131272..62162224hg38UCSC Ensembl
Innerchr2:62358407..62389359hg19UCSC Ensembl
Innerchr2:62211911..62242863hg18UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3830953
hg1930953
hg1830953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3577251
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)nsv1003959
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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