A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004959



Internal ID22066590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74406948..74415359hg38UCSC Ensembl
Outerchr8:74396083..74416300hg38UCSC Ensembl
Innerchr8:75319183..75327594hg19UCSC Ensembl
Outerchr8:75308318..75328535hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3820218
hg1920218
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154368
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004959
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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