A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705569



Internal ID15095535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106580706..106647657hg38UCSC Ensembl
Innerchr14:107036692..107103660hg19UCSC Ensembl
Innerchr14:106107737..106174705hg18UCSC Ensembl
Innerchr14:106107737..106174705hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3866952
hg1966969
hg1866969
hg1766969
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517055
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705569
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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