A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982805



Internal ID20549845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62760661..62760877hg38UCSC Ensembl
chr10:64520421..64520637hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454886
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982805
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00097


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