A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524941



Internal ID18476536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:112483896..112502507hg38UCSC Ensembl
Innerchr12:112921700..112940311hg19UCSC Ensembl
Innerchr12:111406083..111424694hg18UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3818612
hg1918612
hg1818612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043449
Supporting Variants
Samples
Known GenesPTPN11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3524941
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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