A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440287



Internal ID21097840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24125401..24127900hg38UCSC Ensembl
chr10:24414330..24416829hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979243
Samples
Known GenesKIAA1217
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440287
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