A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979607



Internal ID20546647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119305767..119308411hg38UCSC Ensembl
chr10:121065279..121067923hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg382645
hg192645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436489
Supporting Variants
Samples
Known GenesGRK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00143


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