A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3581564



Internal ID18879845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41569117..41703005hg38UCSC Ensembl
Innerchr2:41796257..41930145hg19UCSC Ensembl
Innerchr2:41649761..41783649hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38133889
hg19133889
hg18133889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001428
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3581564
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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