A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149222



Internal ID15853253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57202862..57267189hg38UCSC Ensembl
Innerchr15:57495060..57559387hg19UCSC Ensembl
Innerchr15:55282352..55346679hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3864328
hg1964328
hg1864328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569578
Supporting Variants
Samples1780854023_A
Known GenesTCF12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149222
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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