A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983777



Internal ID20550817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71897819..71908402hg38UCSC Ensembl
chr10:73657577..73668160hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3810584
hg1910584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448140
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983777
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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