A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705690



Internal ID15095656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34275220..34529499hg38UCSC Ensembl
Innerchr14:34744426..34998705hg19UCSC Ensembl
Innerchr14:33814177..34068456hg18UCSC Ensembl
Innerchr14:33814177..34068456hg17UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38254280
hg19254280
hg18254280
hg17254280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528989
Supporting Variants
Samples
Known GenesEAPP, SPTSSA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705690
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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