A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376242



Internal ID22601911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74013918..74017979hg38UCSC Ensembl
chr15:74306259..74310320hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg384062
hg194062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935571
Supporting Variants
Samples
Known GenesPML
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376242
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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