A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525422



Internal ID15452715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:91175890..91228794hg38UCSC Ensembl
Innerchr14:91642234..91695138hg19UCSC Ensembl
Innerchr14:90711987..90764891hg18UCSC Ensembl
Innerchr14:90711987..90764891hg17UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3852905
hg1952905
hg1852905
hg1752905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv141n21
Supporting Variantsnssv701546
Samples
Known GenesC14orf159
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525422
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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