A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639189



Internal ID18937470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:90672809..90923581hg38UCSC Ensembl
Innerchr5:89968626..90219398hg19UCSC Ensembl
Innerchr5:90004382..90255154hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38250773
hg19250773
hg18250773
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015449
Supporting Variants
Samples
Known GenesGPR98
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639189
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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