A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170524



Internal ID22330798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234644722..234650586hg38UCSC Ensembl
chr2:235553366..235559230hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg385865
hg195865
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5055n152
Supporting Variantsnssv14406594, nssv14406595
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3170524
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