A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842725



Internal ID22617660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40981997..40985577hg38UCSC Ensembl
chr5:40982099..40985679hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg383581
hg193581
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499790
Samples
Known GenesC7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842725
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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