A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757497



Internal ID19055778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:137714848..137739157hg38UCSC Ensembl
Innerchr8:138727091..138751400hg19UCSC Ensembl
Innerchr8:138796273..138820582hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3824310
hg1924310
hg1824310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030967
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)nssv3757497
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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