A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097833



Internal ID21407498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58726417..58726417hg38UCSC Ensembl
chr17:56803778..56803778hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646722
Supporting Variants
SamplesHG00512
Known GenesRAD51C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097833
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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