A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354015



Internal ID22579684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57749116..57781322hg38UCSC Ensembl
chr10:59508876..59541082hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3832207
hg1932207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923399
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354015
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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