A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140751



Internal ID20707791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2643675..2653767hg38UCSC Ensembl
chr6:2643909..2654001hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3810093
hg1910093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408609
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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