A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14461314



Internal ID22235446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97436080..97461380hg38UCSC Ensembl
chr7:97065392..97090692hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3825301
hg1925301
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3188822
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14461314
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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