A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002965



Internal ID19092182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:71364462..71404938hg38UCSC Ensembl
Innerchr2:71591592..71632068hg19UCSC Ensembl
Innerchr2:71445100..71485576hg18UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg3840477
hg1940477
hg1840477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3864n100
Supporting Variantsnssv3577293
Samples
Known GenesZNF638
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002965
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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