A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475168



Internal ID22533063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58730367..58731366hg38UCSC Ensembl
chr17:56807728..56808727hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873848
Supporting Variants
Samples
Known GenesRAD51C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475168
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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