A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355338



Internal ID22581007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25312920..25312920hg38UCSC Ensembl
chr1:25639411..25639411hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5956695
Supporting Variants
Samples
Known GenesRHD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355338
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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