A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515567



Internal ID15096174
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702504, nssv703182, nssv695341, nssv663925, nssv681566, nssv695669, nssv702968
Samples
Known GenesDDX1, NBAS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515567
Frequency
Sample Size2026
Observed Gain4
Observed Loss8
Observed Complex0
Frequencyn/a


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