A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435863



Internal ID21093416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26574188..26627785hg38UCSC Ensembl
chr10:26863117..26916714hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3853598
hg1953598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv660n223
Supporting Variantsnssv17981175
Samples
Known GenesLINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435863
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