A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985947



Internal ID20552987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9670405..9856910hg38UCSC Ensembl
chr10:9712368..9898873hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38186506
hg19186506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452989
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985947
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00025


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer