A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842501



Internal ID22617436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178552477..178556788hg38UCSC Ensembl
chr5:177979478..177983789hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384312
hg194312
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495004
Samples
Known GenesCOL23A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842501
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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