A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829800



Internal ID22604735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25310275..25319038hg38UCSC Ensembl
chr1:25636766..25645529hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg388764
hg198764
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464026, nssv17469245
Samples
Known GenesRHD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829800
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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