A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520950



Internal ID21845309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27905878..27905878hg38UCSC Ensembl
chr1:28232389..28232389hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6060298
Supporting Variants
Samples
Known GenesRPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520950
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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