A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv786725



Internal ID15733995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:3198011..3198474hg38UCSC Ensembl
Innerchr12:3307177..3307640hg19UCSC Ensembl
Innerchr12:3177438..3177901hg18UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg38464
hg19464
hg18464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557102
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)nssv786725
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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