A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698143



Internal ID15434795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:92725126..92727981hg38UCSC Ensembl
Innerchr14:93191471..93194326hg19UCSC Ensembl
Innerchr14:92261224..92264079hg18UCSC Ensembl
Innerchr14:92261224..92264079hg17UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg382856
hg192856
hg182856
hg172856
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521526
Supporting Variants
Samples
Known GenesLGMN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698143
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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