A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135327



Internal ID20702367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105626599..105626833hg38UCSC Ensembl
chr6:106074474..106074708hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605815
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135327
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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