A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521452



Internal ID20894813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60719781..60721322hg38UCSC Ensembl
chr17:58797142..58798683hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381542
hg191542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036569
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521452
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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