A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979979



Internal ID20547019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48347914..48353415hg38UCSC Ensembl
chr10:49555957..49561458hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg385502
hg195502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447553
Supporting Variants
Samples
Known GenesMAPK8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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