A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525305



Internal ID20898666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67266201..67269300hg38UCSC Ensembl
chr17:65262317..65265416hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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