A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14402632



Internal ID22305095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141502241..141504732hg38UCSC Ensembl
chr7:141202041..141204532hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg382492
hg192492
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3181113
Supporting Variants
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)nssv14402632
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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