A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451002



Internal ID21108555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87730210..87770942hg38UCSC Ensembl
chr10:89489967..89530699hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3840733
hg1940733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984810
Samples
Known GenesATAD1, PAPSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451002
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