A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680069



Internal ID15416721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:123915199..123939593hg38UCSC Ensembl
Innerchr3:123634046..123658440hg19UCSC Ensembl
Innerchr3:125116736..125141130hg18UCSC Ensembl
Innerchr3:125116736..125141130hg17UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3824395
hg1924395
hg1824395
hg1724395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520308
Supporting Variants
Samples
Known GenesCCDC14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680069
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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