A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987176



Internal ID20554218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118062082..118137025hg38UCSC Ensembl
chr11:117932797..118007740hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3874944
hg1974944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456102
Supporting Variants
Samples
Known GenesSCN4B, TMPRSS4, TMPRSS4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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