A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151190



Internal ID15880928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240442666..240471872hg38UCSC Ensembl
Innerchr2:241382083..241411289hg19UCSC Ensembl
Innerchr2:241030756..241059962hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3829207
hg1929207
hg1829207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584810
Supporting Variants
SamplesNINDS_49
Known GenesGPC1, MIR149, PP14571
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151190
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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