A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3175595



Internal ID22333444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51017027..51017100hg38UCSC Ensembl
chr5:50312861..50312934hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14399771
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3175595
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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