A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525655



Internal ID15452948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:91175890..91233074hg38UCSC Ensembl
Innerchr14:91642234..91699418hg19UCSC Ensembl
Innerchr14:90711987..90769171hg18UCSC Ensembl
Innerchr14:90711987..90769171hg17UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3857185
hg1957185
hg1857185
hg1757185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv141n21
Supporting Variantsnssv701810
Samples
Known GenesC14orf159, GPR68
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525655
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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