A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441192



Internal ID21098745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26584858..26641185hg38UCSC Ensembl
chr10:26873787..26930114hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3856328
hg1956328
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv662n223
Supporting Variantsnssv18191720
Samples
Known GenesLINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer