A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730900



Internal ID20506816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68831847..68831944hg38UCSC Ensembl
chr15:69124186..69124283hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268342
Samples
Known GenesMIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730900
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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