A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691517



Internal ID18989798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:127489522..127521674hg38UCSC Ensembl
Innerchr8:128501767..128533919hg19UCSC Ensembl
Innerchr8:128570949..128603101hg18UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3832153
hg1932153
hg1832153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023264
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)nssv3691517
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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