A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992656



Internal ID20559696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60674301..60676000hg38UCSC Ensembl
chr11:60441774..60443473hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466186
Supporting Variants
Samples
Known GenesLINC00301
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992656
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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