A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703696



Internal ID15440348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:59311543..59314926hg38UCSC Ensembl
Innerchr14:59778261..59781644hg19UCSC Ensembl
Innerchr14:58848014..58851397hg18UCSC Ensembl
Innerchr14:58848014..58851397hg17UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg383384
hg193384
hg183384
hg173384
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527284
Supporting Variants
Samples
Known GenesDAAM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703696
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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