A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350607



Internal ID22576276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101059241..101059490hg38UCSC Ensembl
chr10:102818998..102819247hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921700
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350607
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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