A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3171779



Internal ID22331470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157309853..157314391hg38UCSC Ensembl
chr6:157730885..157735423hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384539
hg194539
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14453406
SamplesHG00733
Known GenesTMEM242
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3171779
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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