A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471780



Internal ID22529672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73346635..73348934hg38UCSC Ensembl
chr15:73638976..73641275hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852013
Supporting Variants
Samples
Known GenesHCN4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471780
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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