A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830192



Internal ID22605127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3900717..3909641hg38UCSC Ensembl
chr1:3817281..3826205hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg388925
hg198925
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450335
Samples
Known GenesLINC01134
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830192
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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