A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3173210



Internal ID22332206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27332897..27333261hg38UCSC Ensembl
chr1:27659388..27659752hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14413847
SamplesHG00514
Known GenesTMEM222
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3173210
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer