A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701922



Internal ID15438574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20014312..20033153hg38UCSC Ensembl
Innerchr14:20482471..20501312hg19UCSC Ensembl
Innerchr14:19552311..19571152hg18UCSC Ensembl
Innerchr14:19552311..19571152hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3818842
hg1918842
hg1818842
hg1718842
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525754
Supporting Variants
Samples
Known GenesOR4K14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701922
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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