A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518509



Internal ID20891870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62115535..62151141hg38UCSC Ensembl
chr17:60192896..60228502hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3835607
hg1935607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer