A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14402929



Internal ID22297684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101228957..101252525hg38UCSC Ensembl
chr13:101881308..101904876hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3823569
hg1923569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3221533
Supporting Variants
SamplesNA19240
Known GenesNALCN
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14402929
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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