A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441996



Internal ID21099549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97577242..97579410hg38UCSC Ensembl
chr10:99336999..99339167hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg382169
hg192169
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189015
Samples
Known GenesANKRD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441996
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