A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3179635



Internal ID22335659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177468013..177468069hg38UCSC Ensembl
chr5:176895014..176895070hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14460099
SamplesHG00733
Known GenesDBN1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3179635
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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