A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036832



Internal ID20603872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61295614..61300985hg38UCSC Ensembl
chr17:59372975..59378346hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg385372
hg195372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533481
Supporting Variants
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036832
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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