A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736980



Internal ID20512935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60819018..60819088hg38UCSC Ensembl
chr5:60114845..60114915hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270812
Samples
Known GenesELOVL7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736980
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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