A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516767



Internal ID15444060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17737040..17788177hg38UCSC Ensembl
Innerchr11:17758587..17809724hg19UCSC Ensembl
Innerchr11:17715163..17766300hg18UCSC Ensembl
Innerchr11:17715163..17766300hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3851138
hg1951138
hg1851138
hg1751138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv670708, nssv687100, nssv682282, nssv660208
Samples
Known GenesKCNC1, SERGEF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516767
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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