A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150597



Internal ID20717637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97707371..97713745hg38UCSC Ensembl
chr6:98155247..98161621hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg386375
hg196375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616760
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150597
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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