A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729125



Internal ID19027406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91733767..92117746hg38UCSC Ensembl
Innerchr2:91921793..92305772hg19UCSC Ensembl
Innerchr2:91285520..91669499hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38383980
hg19383980
hg18383980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010987
Supporting Variants
Samples
Known GenesACTR3BP2, GGT8P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3729125
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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