A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019383



Internal ID19108601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131602420..131642575hg38UCSC Ensembl
Innerchr8:132614667..132654822hg19UCSC Ensembl
Innerchr8:132683849..132724004hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3840156
hg1940156
hg1840156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7313n100
Supporting Variantsnssv3691530
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)nsv1019383
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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