A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367900



Internal ID22593569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61156826..61156978hg38UCSC Ensembl
chr11:60924298..60924450hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915970
Supporting Variants
Samples
Known GenesVPS37C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367900
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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