A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv783385



Internal ID15730655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106806216..106833524hg38UCSC Ensembl
Innerchr11:106676942..106704250hg19UCSC Ensembl
Innerchr11:106182152..106209460hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3827309
hg1927309
hg1827309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556230
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)nssv783385
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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