A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064903



Internal ID18807434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84386735..84500091hg38UCSC Ensembl
Innerchr16:84420341..84533697hg19UCSC Ensembl
Innerchr16:82977842..83091198hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38113357
hg19113357
hg18113357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3057n100
Supporting Variantsnssv3559950
Samples
Known GenesATP2C2, TLDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064903
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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