A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680301



Internal ID15416953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134505414..134751116hg38UCSC Ensembl
Innerchr11:134375308..134621010hg19UCSC Ensembl
Innerchr11:133880518..134126220hg18UCSC Ensembl
Innerchr11:133880518..134126220hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38245703
hg19245703
hg18245703
hg17245703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517742
Supporting Variants
Samples
Known GenesLOC283177
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680301
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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