A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3185857



Internal ID22338885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210389085..210389174hg38UCSC Ensembl
chr1:210562429..210562518hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14459237
SamplesHG00733
Known GenesHHAT
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3185857
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