A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731801



Internal ID20507722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55105986..55106249hg38UCSC Ensembl
chr5:54401814..54402077hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274416
Samples
Known GenesGZMA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731801
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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