A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982771



Internal ID20549811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61359585..61360212hg38UCSC Ensembl
chr10:63119343..63119970hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451330
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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