A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522850



Internal ID15103457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21521707..21529974hg38UCSC Ensembl
Innerchr14:21989841..21998108hg19UCSC Ensembl
Innerchr14:21059681..21067948hg18UCSC Ensembl
Innerchr14:21059681..21067948hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg388268
hg198268
hg188268
hg178268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698503
Samples
Known GenesSALL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522850
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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