A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501887



Internal ID20875125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1856805..1858671hg38UCSC Ensembl
chr17:1760099..1761965hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381867
hg191867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034129
Samples
Known GenesRPA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501887
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