A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530452



Internal ID20903813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68401887..68406810hg38UCSC Ensembl
chr17:66398028..66402951hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg384924
hg194924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037540
Samples
Known GenesARSG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530452
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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