A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369218



Internal ID22594887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90949978..90979231hg38UCSC Ensembl
chr10:92709735..92738988hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3829254
hg1929254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369218
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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