A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515889



Internal ID20889250
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 StatusM
Merged Variants
Supporting Variantsnssv18036654
Samples
Known GenesKIF2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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