A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv786726



Internal ID15733996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:3198011..3198529hg38UCSC Ensembl
Innerchr12:3307177..3307695hg19UCSC Ensembl
Innerchr12:3177438..3177956hg18UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg38519
hg19519
hg18519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557103
Supporting Variants
Samples
Known GenesTSPAN9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv786726
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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