A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524324



Internal ID20897685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64011674..64018226hg38UCSC Ensembl
chr17:62089034..62095586hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg386553
hg196553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037745
Samples
Known GenesICAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524324
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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