A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471822



Internal ID22529714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41920609..41930187hg38UCSC Ensembl
chr15:42212807..42222385hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg389579
hg199579
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854349
Supporting Variants
Samples
Known GenesEHD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471822
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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