A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582822



Internal ID18881103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:144049353..144212251hg38UCSC Ensembl
Innerchr2:144806920..144969818hg19UCSC Ensembl
Innerchr2:144523390..144686288hg18UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg38162899
hg19162899
hg18162899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013338
Supporting Variants
Samples
Known GenesGTDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3582822
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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