A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360228



Internal ID22585897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25287187..25405613hg38UCSC Ensembl
chr1:25613678..25732104hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38118427
hg19118427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870847
Supporting Variants
Samples
Known GenesRHCE, RHD, TMEM50A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360228
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.04


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