A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982610



Internal ID20549650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6188852..6189548hg38UCSC Ensembl
chr10:6230815..6231511hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445320
Supporting Variants
Samples
Known GenesPFKFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982610
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00036


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