A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694527



Internal ID15431179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76000853..76039532hg38UCSC Ensembl
Innerchr11:75711897..75750576hg19UCSC Ensembl
Innerchr11:75389545..75428224hg18UCSC Ensembl
Innerchr11:75389545..75428224hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3838680
hg1938680
hg1838680
hg1738680
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515973
Supporting Variants
Samples
Known GenesUVRAG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694527
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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