A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979421



Internal ID20546461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36076267..36081690hg38UCSC Ensembl
chr10:36365195..36370618hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg385424
hg195424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442880
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979421
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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