A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350599



Internal ID22576268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124551016..124551957hg38UCSC Ensembl
chr10:126239585..126240526hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38942
hg19942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910932
Supporting Variants
Samples
Known GenesLHPP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350599
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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