A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980025



Internal ID20547065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49513367..49514131hg38UCSC Ensembl
chr10:50721413..50722177hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436920
Supporting Variants
Samples
Known GenesERCC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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