A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702541



Internal ID15092507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77977728..77987478hg38UCSC Ensembl
Innerchr11:77688774..77698524hg19UCSC Ensembl
Innerchr11:77366422..77376172hg18UCSC Ensembl
Innerchr11:77366422..77376172hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg389751
hg199751
hg189751
hg179751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526268
Supporting Variants
Samples
Known GenesINTS4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702541
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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