A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056858



Internal ID18799389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55514410..55549536hg38UCSC Ensembl
Innerchr16:55548322..55583448hg19UCSC Ensembl
Innerchr16:54105823..54140949hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3835127
hg1935127
hg1835127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2982n100
Supporting Variantsnssv3559281
Samples
Known GenesLPCAT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056858
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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