A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999262



Internal ID19158798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41587034..41624260hg38UCSC Ensembl
Innerchr2:41814174..41851400hg19UCSC Ensembl
Innerchr2:41667678..41704904hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3837227
hg1937227
hg1837227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3796n100
Supporting Variantsnssv3725980
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)nsv999262
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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