A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437653



Internal ID21095206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26582722..26640993hg38UCSC Ensembl
chr10:26871651..26929922hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3858272
hg1958272
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv662n223
Supporting Variantsnssv18187417
Samples
Known GenesLINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437653
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