A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979490



Internal ID20546530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1102043..1102107hg38UCSC Ensembl
chr10:1147983..1148047hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451205
Supporting Variants
Samples
Known GenesWDR37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979490
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer