A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992505



Internal ID20559545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60412001..60413500hg38UCSC Ensembl
chr11:60179474..60180973hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474824
Supporting Variants
Samples
Known GenesMS4A14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992505
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0014


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