A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021597



Internal ID19110815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:122449335..122467565hg38UCSC Ensembl
Innerchr8:123461574..123479804hg19UCSC Ensembl
Innerchr8:123530755..123548985hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3818231
hg1918231
hg1818231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7305n100
Supporting Variantsnssv3691490
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)nsv1021597
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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