A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984054



Internal ID20551094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75408001..75408600hg38UCSC Ensembl
chr10:77167759..77168358hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448039
Supporting Variants
Samples
Known GenesZNF503-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984054
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03308


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