A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990802



Internal ID20557842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3367001..3368200hg38UCSC Ensembl
chr11:3388231..3389430hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443978
Supporting Variants
Samples
Known GenesZNF195
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00347


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