A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3173965



Internal ID22332570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168228148..168228205hg38UCSC Ensembl
chr5:167655153..167655210hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14466067
SamplesHG00733
Known GenesTENM2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3173965
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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