A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472831



Internal ID22530723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51577497..51581096hg38UCSC Ensembl
chr15:51869694..51873293hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864665
Supporting Variants
Samples
Known GenesDMXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472831
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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