A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524908



Internal ID8419183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:64233327..64236875hg38UCSC Ensembl
Innerchr14:64700045..64703593hg19UCSC Ensembl
Innerchr14:63769798..63773346hg18UCSC Ensembl
Innerchr14:63769798..63773346hg17UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg383549
hg193549
hg183549
hg173549
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700919
Samples
Known GenesESR2, MIR548AZ
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524908
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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