A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982877



Internal ID20549917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64956817..64966380hg38UCSC Ensembl
chr10:66716575..66726138hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg389564
hg199564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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