A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019200



Internal ID19108418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:135650976..135874995hg38UCSC Ensembl
Innerchr8:136663219..136887238hg19UCSC Ensembl
Innerchr8:136732401..136956420hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38224020
hg19224020
hg18224020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692720
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)nsv1019200
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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