A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3185149



Internal ID22338521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169744714..169744982hg38UCSC Ensembl
chr6:170144810..170145078hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14467228
SamplesHG00733
Known GenesTCTE3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3185149
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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