A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442442



Internal ID21099995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15024987..15039316hg38UCSC Ensembl
chr10:15066986..15081315hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3814330
hg1914330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442442
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