A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175896



Internal ID15876474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:115456385..115497519hg38UCSC Ensembl
Innerchr12:115894190..115935324hg19UCSC Ensembl
Innerchr12:114378573..114419707hg18UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3841135
hg1941135
hg1841135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560307
Supporting Variants
SamplesHGDP00847
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175896
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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