A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350140



Internal ID22575809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1094786..1094912hg38UCSC Ensembl
chr10:1140726..1140852hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923986
Supporting Variants
Samples
Known GenesWDR37
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350140
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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