A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021038



Internal ID19110256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9949314..9984724hg38UCSC Ensembl
Innerchr8:9806824..9842234hg19UCSC Ensembl
Innerchr8:9844234..9879644hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3835411
hg1935411
hg1835411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681710
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)nsv1021038
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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