A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141292



Internal ID20708332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25762811..25763341hg38UCSC Ensembl
chr6:25763039..25763569hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404310
Supporting Variants
Samples
Known GenesSLC17A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141292
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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