A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757498



Internal ID19055779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139119592..139139175hg38UCSC Ensembl
Innerchr8:140131835..140151418hg19UCSC Ensembl
Innerchr8:140201017..140220600hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3819584
hg1919584
hg1819584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024030
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)nssv3757498
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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