A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447309



Internal ID21104862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92298712..92307724hg38UCSC Ensembl
chr10:94058469..94067481hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg389013
hg199013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985405
Samples
Known GenesMARCH5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447309
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