A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372358



Internal ID22598027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49880094..49906469hg38UCSC Ensembl
chr15:50172291..50198666hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3826376
hg1926376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945785
Supporting Variants
Samples
Known GenesATP8B4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372358
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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