A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576953



Internal ID18875234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9889943..9912128hg38UCSC Ensembl
Innerchr2:10030072..10052257hg19UCSC Ensembl
Innerchr2:9947523..9969708hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3822186
hg1922186
hg1822186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009210
Supporting Variants
Samples
Known GenesTAF1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3576953
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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