A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3182138



Internal ID22336936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168377722..168381791hg38UCSC Ensembl
chr6:168778402..168782471hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg384070
hg194070
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14375867, nssv14382821
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)nsv3182138
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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