A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150487



Internal ID15526063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:110143318..110217118hg38UCSC Ensembl
Innerchr2:110900895..110974695hg19UCSC Ensembl
Innerchr2:110258184..110331984hg18UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3873801
hg1973801
hg1873801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582691
Supporting Variants
SamplesHGDP00029
Known GenesLINC00116, NPHP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150487
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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