A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841620



Internal ID22616555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177434181..177441292hg38UCSC Ensembl
chr5:176861182..176868293hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg387112
hg197112
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498382
Samples
Known GenesGRK6, PRR7-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841620
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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