A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025376



Internal ID19114594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131202546..131269646hg38UCSC Ensembl
Innerchr8:132214793..132281893hg19UCSC Ensembl
Innerchr8:132283975..132351075hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3867101
hg1967101
hg1867101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691529
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)nsv1025376
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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