A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347128



Internal ID22120468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82510414..82510484hg38UCSC Ensembl
chr9:85125329..85125399hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220719
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347128
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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