A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140160



Internal ID20707200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142530944..142531305hg38UCSC Ensembl
chr6:142852081..142852442hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611560
Supporting Variants
Samples
Known GenesLOC153910
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140160
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00282


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