A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526040



Internal ID20899401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59654411..59654693hg38UCSC Ensembl
chr17:57731772..57732054hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036381
Samples
Known GenesCLTC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526040
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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