A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516826



Internal ID20890187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:52536046..52659872hg38UCSC Ensembl
chr17:50613406..50737232hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38123827
hg19123827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516826
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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