A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv913432



Internal ID16207388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77311466..77362775hg38UCSC Ensembl
Innerchr2:77538592..77589901hg19UCSC Ensembl
Innerchr2:77392100..77443409hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3851310
hg1951310
hg1851310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582254
Supporting Variants
Samples
Known GenesLRRTM4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv913432
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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