A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436786



Internal ID21094339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116824800..116825791hg38UCSC Ensembl
chr10:118584311..118585302hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436786
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