A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681566



Internal ID15071532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14864624..15766654hg38UCSC Ensembl
Innerchr2:15004748..15906778hg19UCSC Ensembl
Innerchr2:14922199..15824229hg18UCSC Ensembl
Innerchr2:14955346..15857376hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38902031
hg19902031
hg18902031
hg17902031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515567
Supporting Variants
Samples
Known GenesDDX1, NBAS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681566
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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