A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841665



Internal ID22616600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132419605..132436605hg38UCSC Ensembl
chr5:131755297..131772297hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3817001
hg1917001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494933
Samples
Known GenesC5orf56
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841665
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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