A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3175170



Internal ID22333211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5205375..5205866hg38UCSC Ensembl
chr1:5265435..5265926hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14440037
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3175170
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