A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3638077



Internal ID18936358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99981336..100112652hg38UCSC Ensembl
Innerchr5:99317040..99448356hg19UCSC Ensembl
Innerchr5:99344939..99476255hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38131317
hg19131317
hg18131317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031008
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)nssv3638077
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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