A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532254



Internal ID20905615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63702090..63709391hg38UCSC Ensembl
chr17:61779450..61786751hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg387302
hg197302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037252
Samples
Known GenesLOC729683, STRADA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532254
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