A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505499



Internal ID20878769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1424268..1428242hg38UCSC Ensembl
chr17:1327562..1331536hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg383975
hg193975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034371
Samples
Known GenesCRK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505499
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