A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516379



Internal ID20889740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68087704..68182450hg38UCSC Ensembl
chr17:66083844..66178591hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3894747
hg1994748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037460
Samples
Known GenesLINC00674
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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