A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141937



Internal ID20708977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157261953..157265632hg38UCSC Ensembl
chr6:157614001..157617680hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383680
hg193680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611118
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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