A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742662



Internal ID20518647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201924412..201924513hg38UCSC Ensembl
chr1:201893540..201893641hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273269
Samples
Known GenesLMOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742662
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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