A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681563



Internal ID15071529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90537591..90598496hg38UCSC Ensembl
Innerchr7:90166905..90227810hg19UCSC Ensembl
Innerchr7:90004841..90065746hg18UCSC Ensembl
Innerchr7:89811556..89872461hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3860906
hg1960906
hg1860906
hg1760906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515998
Supporting Variants
Samples
Known GenesCDK14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681563
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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