A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472362



Internal ID22530254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84869628..84883245hg38UCSC Ensembl
chr15:85412859..85426476hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3813618
hg1913618
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848536
Supporting Variants
Samples
Known GenesALPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472362
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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