A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3637069



Internal ID18935350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:35446107..35491083hg38UCSC Ensembl
Innerchr5:35446209..35491185hg19UCSC Ensembl
Innerchr5:35481966..35526942hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3844977
hg1944977
hg1844977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018541
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)nssv3637069
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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