A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985271



Internal ID20552312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94561801..94569200hg38UCSC Ensembl
chr10:96321558..96328957hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444655
Supporting Variants
Samples
Known GenesHELLS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985271
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00104


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