A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14411484



Internal ID22326074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95504265..95504649hg38UCSC Ensembl
chr5:94839969..94840353hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3187501
Supporting Variants
SamplesNA19240
Known GenesTTC37
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14411484
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