A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036827



Internal ID20603867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61240415..61242024hg38UCSC Ensembl
chr17:59317776..59319385hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381610
hg191610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516240
Supporting Variants
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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