A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830125



Internal ID22605060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67104946..67107392hg38UCSC Ensembl
chr1:67570629..67573075hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg382447
hg192447
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481150, nssv17481151
Samples
Known GenesC1orf141
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830125
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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