A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2766490



Internal ID17537357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106915593..106922923hg38UCSC Ensembl
Innerchr11:106786319..106793649hg19UCSC Ensembl
Innerchr11:106291529..106298859hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg387331
hg197331
hg187331
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv983210
Supporting Variants
SamplesHGDP01307
Known GenesGUCY1A2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2766490
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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