A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730779



Internal ID20506693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58726422..58726567hg38UCSC Ensembl
chr17:56803783..56803928hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293218
Samples
Known GenesRAD51C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730779
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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