A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14461482



Internal ID22214076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97867019..97867348hg38UCSC Ensembl
chr7:97496331..97496660hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3181818
Supporting Variants
SamplesHG00733
Known GenesASNS
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14461482
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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