A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360242



Internal ID22585911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128626694..128634622hg38UCSC Ensembl
chr10:130424958..130432886hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg387929
hg197929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919469
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360242
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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