A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14333029



Internal ID22120560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22029512..22032027hg38UCSC Ensembl
chr7:22069130..22071645hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg382516
hg192516
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3234017
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14333029
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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