A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2763580



Internal ID17537199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8895187..8901517hg38UCSC Ensembl
Innerchr8:8752697..8759027hg19UCSC Ensembl
Innerchr8:8790107..8796437hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386331
hg196331
hg186331
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972228
Supporting Variants
SamplesHGDP01307
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2763580
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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