A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358580



Internal ID22584249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123999741..123999878hg38UCSC Ensembl
chr10:125759257..125759394hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923799
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358580
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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