A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515768



Internal ID15096375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:118089712..118091193hg38UCSC Ensembl
Innerchr11:117960427..117961908hg19UCSC Ensembl
Innerchr11:117465637..117467118hg18UCSC Ensembl
Innerchr11:117465637..117467118hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381482
hg191482
hg181482
hg171482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664722, nssv685028, nssv678720
Samples
Known GenesTMPRSS4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515768
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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