A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737162



Internal ID20513120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65613467..65613747hg38UCSC Ensembl
chr1:66079150..66079430hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284865
Samples
Known GenesLEPR
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737162
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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