A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989815



Internal ID20556855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27496901..27498300hg38UCSC Ensembl
chr11:27518448..27519847hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439847
Supporting Variants
Samples
Known GenesLIN7C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989815
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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