A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440602



Internal ID21098155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69944393..69945810hg38UCSC Ensembl
chr10:71704149..71705566hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381418
hg191418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983512
Samples
Known GenesCOL13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440602
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