A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3172522



Internal ID22331848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7230623..7230688hg38UCSC Ensembl
chr4:7232350..7232415hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14434755, nssv14454320
SamplesHG00733, HG00514
Known GenesSORCS2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3172522
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