A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2756856



Internal ID17817237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81158501..81170101hg38UCSC Ensembl
Innerchr11:80869544..80881144hg19UCSC Ensembl
Innerchr11:80547192..80558792hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3811601
hg1911601
hg1811601
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv983208
Supporting Variants
SamplesHGDP00927
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2756856
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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