A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357257



Internal ID22582926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86626970..86635423hg38UCSC Ensembl
chr10:88386727..88395180hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg388454
hg198454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915468
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357257
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