A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828267



Internal ID22603202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161318924..161352890hg38UCSC Ensembl
chr1:161288714..161322680hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3833967
hg1933967
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465873
Samples
Known GenesSDHC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828267
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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