A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718955



Internal ID18670550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14954899..15009807hg38UCSC Ensembl
Innerchr16:15048756..15103664hg19UCSC Ensembl
Innerchr16:14956257..15011165hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3854909
hg1954909
hg1854909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047003
Supporting Variants
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)nssv3718955
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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