A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436289



Internal ID21093842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71658716..71664151hg38UCSC Ensembl
chr10:73418473..73423908hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg385436
hg195436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983769
Samples
Known GenesCDH23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436289
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