A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599362



Internal ID18897643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7528721..7586265hg38UCSC Ensembl
Innerchr20:7509368..7566912hg19UCSC Ensembl
Innerchr20:7457368..7514912hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3857545
hg1957545
hg1857545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062661
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)nssv3599362
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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