A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024575



Internal ID19113792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:58188689..58228451hg38UCSC Ensembl
Innerchr8:59101248..59141010hg19UCSC Ensembl
Innerchr8:59263802..59303564hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3839763
hg1939763
hg1839763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689454
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)nsv1024575
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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