A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3647099



Internal ID18945380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:116197368..116273855hg38UCSC Ensembl
Innerchr5:115533065..115609552hg19UCSC Ensembl
Innerchr5:115560964..115637451hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3876488
hg1976488
hg1876488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032799
Supporting Variants
Samples
Known GenesCOMMD10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3647099
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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