A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980043



Internal ID20547083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32155139..32164964hg38UCSC Ensembl
chr10:32444067..32453892hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg389826
hg199826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452795
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980043
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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