A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834769



Internal ID15782039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105305091..105475240hg38UCSC Ensembl
Innerchr14:105771428..105941577hg19UCSC Ensembl
Innerchr14:104842473..105012622hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38170150
hg19170150
hg18170150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566189
Supporting Variants
Samples
Known GenesBRF1, CRIP2, MTA1, PACS2, TEX22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834769
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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