A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535455



Internal ID20908816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60376601..60391100hg38UCSC Ensembl
chr17:58453962..58468461hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3814500
hg1914500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036544
Samples
Known GenesUSP32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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