A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520815



Internal ID20894176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58170247..58180898hg38UCSC Ensembl
chr17:56247608..56258259hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3810652
hg1910652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036295
Samples
Known GenesOR4D2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520815
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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