A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736250



Internal ID20512197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78498135..78498339hg38UCSC Ensembl
chr5:77793958..77794162hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261939
Samples
Known GenesLHFPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736250
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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