A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3181939



Internal ID22336830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36102343..36102417hg38UCSC Ensembl
chr6:36070120..36070194hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14435652
SamplesHG00514
Known GenesMAPK14
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3181939
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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