A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175894



Internal ID15877887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:115087270..115105654hg38UCSC Ensembl
Innerchr12:115525075..115543459hg19UCSC Ensembl
Innerchr12:114009458..114027842hg18UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3818385
hg1918385
hg1818385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560296
Supporting Variants
SamplesHGDP01063
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175894
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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