A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941072



Internal ID21361141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58493539..58493601hg38UCSC Ensembl
chr15:58785738..58785800hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183810
SamplesHG002
Known GenesLIPC
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941072
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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