A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv783624



Internal ID15730894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106915897..106918150hg38UCSC Ensembl
Innerchr11:106786623..106788876hg19UCSC Ensembl
Innerchr11:106291833..106294086hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg382254
hg192254
hg182254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556251
Supporting Variants
Samples
Known GenesGUCY1A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv783624
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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