A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982082



Internal ID20549122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52219816..52220644hg38UCSC Ensembl
chr10:53979576..53980404hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38829
hg19829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439102
Supporting Variants
Samples
Known GenesPRKG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982082
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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