A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031870



Internal ID19121092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83107376..83212876hg38UCSC Ensembl
Innerchr8:84019611..84125111hg19UCSC Ensembl
Innerchr8:84182166..84287666hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38105501
hg19105501
hg18105501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7247n100
Supporting Variantsnssv3689599
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)nsv1031870
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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