A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743541



Internal ID20519529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108043543..108043685hg38UCSC Ensembl
chr7:107683988..107684130hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295587
Samples
Known GenesLAMB4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743541
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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