A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992774



Internal ID20559814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7219912..7220332hg38UCSC Ensembl
chr11:7241143..7241563hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448464
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00126


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