A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176305



Internal ID15529849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52009326..52047766hg38UCSC Ensembl
Innerchr12:52403110..52441550hg19UCSC Ensembl
Innerchr12:50689377..50727817hg18UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3838441
hg1938441
hg1838441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558896
Supporting Variants
SamplesHGDP00857
Known GenesGRASP, NR4A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176305
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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