A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524445



Internal ID20897806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60779501..60790900hg38UCSC Ensembl
chr17:58856862..58868261hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3811400
hg1911400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3209n223
Supporting Variantsnssv18036570
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524445
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