A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042379



Internal ID18784910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14956016..15009807hg38UCSC Ensembl
Innerchr16:15049873..15103664hg19UCSC Ensembl
Innerchr16:14957374..15011165hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3853792
hg1953792
hg1853792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2763n100
Supporting Variantsnssv3557839
Samples
Known GenesPDXDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042379
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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