A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984586



Internal ID20551626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84167671..84172371hg38UCSC Ensembl
chr10:85927427..85932127hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg384701
hg194701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440798
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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