A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464026



Internal ID22521912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25310275..25319038hg38UCSC Ensembl
chr1:25636766..25645529hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg388764
hg198764
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829800
Supporting Variants
Samples
Known GenesRHD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464026
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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