A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136884



Internal ID20703924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106700523..106701441hg38UCSC Ensembl
chr6:107148398..107149316hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608673
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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