A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693873



Internal ID15083839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105136282..105532207hg38UCSC Ensembl
Innerchr14:105602619..105998544hg19UCSC Ensembl
Innerchr14:104673664..105069589hg18UCSC Ensembl
Innerchr14:104673664..105069589hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38395926
hg19395926
hg18395926
hg17395926
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517055
Supporting Variants
Samples
Known GenesBRF1, BTBD6, C14orf80, CRIP1, CRIP2, JAG2, MIR6765, MTA1, NUDT14, PACS2, TEX22, TMEM121
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693873
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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