A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698441



Internal ID15088407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104699665..104719329hg38UCSC Ensembl
Innerchr14:105166002..105185666hg19UCSC Ensembl
Innerchr14:104237047..104256711hg18UCSC Ensembl
Innerchr14:104237047..104256711hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3819665
hg1919665
hg1819665
hg1719665
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517038
Supporting Variants
Samples
Known GenesINF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698441
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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