A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335524



Internal ID22210441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97445822..97460380hg38UCSC Ensembl
chr7:97075134..97089692hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3814559
hg1914559
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3558313
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335524
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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