A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454778



Internal ID21112331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119773993..119780303hg38UCSC Ensembl
chr10:121533505..121539815hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg386311
hg196311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980455
Samples
Known GenesINPP5F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454778
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