A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660452



Internal ID15050418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:90532857..90554164hg38UCSC Ensembl
Innerchr14:90999201..91020508hg19UCSC Ensembl
Innerchr14:90068954..90090261hg18UCSC Ensembl
Innerchr14:90068954..90090261hg17UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3821308
hg1921308
hg1821308
hg1721308
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520068
Supporting Variants
Samples
Known GenesTTC7B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660452
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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