A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515998



Internal ID15096605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90471292..90598496hg38UCSC Ensembl
Innerchr7:90100606..90227810hg19UCSC Ensembl
Innerchr7:89938542..90065746hg18UCSC Ensembl
Innerchr7:89745257..89872461hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38127205
hg19127205
hg18127205
hg17127205
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677433, nssv674797, nssv665640, nssv681563, nssv657362
Samples
Known GenesCDK14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515998
Frequency
Sample Size2026
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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