A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005938



Internal ID19095156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9903052..9934255hg38UCSC Ensembl
Innerchr2:10043181..10074384hg19UCSC Ensembl
Innerchr2:9960632..9991835hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3831204
hg1931204
hg1831204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3576956
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)nsv1005938
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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