A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv801680



Internal ID16095636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:101711211..101713006hg38UCSC Ensembl
Innerchr12:102104989..102106784hg19UCSC Ensembl
Innerchr12:100629120..100630915hg18UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg381796
hg191796
hg181796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560010
Supporting Variants
Samples
Known GenesCHPT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv801680
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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