A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532630



Internal ID20905991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48968383..48971350hg38UCSC Ensembl
chr17:47045745..47048712hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg382968
hg192968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036096
Samples
Known GenesGIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532630
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