A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436920



Internal ID21094473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49513367..49514131hg38UCSC Ensembl
chr10:50721413..50722177hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980025
Samples
Known GenesERCC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436920
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