A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979928



Internal ID20546968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37648767..37652233hg38UCSC Ensembl
chr10:37937695..37941161hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg383467
hg193467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439863
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979928
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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