A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983866



Internal ID20550906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73523..74507hg38UCSC Ensembl
chr10:119463..120447hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983866
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02594


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