A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2765448



Internal ID17822263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:32117205..32134841hg38UCSC Ensembl
Innerchr11:32138751..32156387hg19UCSC Ensembl
Innerchr11:32095327..32112963hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3817637
hg1917637
hg1817637
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv983205
Supporting Variants
SamplesHGDP00927
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2765448
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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