A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008906



Internal ID19098124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:23773045..23828447hg38UCSC Ensembl
Innerchr2:23995915..24051317hg19UCSC Ensembl
Innerchr2:23849419..23904821hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3855403
hg1955403
hg1855403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3579017
Samples
Known GenesATAD2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008906
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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