A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520068



Internal ID15100675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:90502030..90560888hg38UCSC Ensembl
Innerchr14:90968374..91027232hg19UCSC Ensembl
Innerchr14:90038127..90096985hg18UCSC Ensembl
Innerchr14:90038127..90096985hg17UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3858859
hg1958859
hg1858859
hg1758859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677917, nssv674232, nssv702552, nssv691223, nssv691749, nssv660452, nssv683162
Samples
Known GenesTTC7B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520068
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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