A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036654



Internal ID20603694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53775201..53886840hg38UCSC Ensembl
chr17:51852562..51964201hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38111640
hg19111640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515889
Supporting Variants
Samples
Known GenesKIF2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036654
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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