A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019671



Internal ID19108889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88381589..88431163hg38UCSC Ensembl
Innerchr8:89393818..89443392hg19UCSC Ensembl
Innerchr8:89462934..89512508hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3849575
hg1949575
hg1849575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7264n100
Supporting Variantsnssv3757321
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)nsv1019671
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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