A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443077



Internal ID21100630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100595801..100602300hg38UCSC Ensembl
chr10:102355558..102362057hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv871n223
Supporting Variantsnssv17977147
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443077
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