A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993618



Internal ID20560658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7473049..7475053hg38UCSC Ensembl
chr11:7494280..7496284hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382005
hg192005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439457
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993618
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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