A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944156



Internal ID22719616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67287523..67290747hg38UCSC Ensembl
chr15:67579861..67583085hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383225
hg193225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381621
Samples
Known GenesIQCH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944156
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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