A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732744



Internal ID20508669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61505692..61505777hg38UCSC Ensembl
chr17:59583053..59583138hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732744
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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