A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977184



Internal ID20544224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101258878..101264772hg38UCSC Ensembl
chr10:103018635..103024529hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg385895
hg195895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437408
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977184
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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