A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280833



Internal ID20490051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84165777..84244697hg38UCSC Ensembl
chr15:84834529..84913449hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3878921
hg1978921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747557
Supporting Variants
Samples
Known GenesGOLGA6L4, LOC100505679, LOC388152, LOC440300, LOC642423
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280833
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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