A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828377



Internal ID22603312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159968040..159974023hg38UCSC Ensembl
chr1:159937830..159943813hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg385984
hg195984
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454313
Samples
Known GenesLINC01133
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828377
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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