A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14336052



Internal ID22197021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91481359..91508180hg38UCSC Ensembl
chr7:91110674..91137495hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3826822
hg1926822
Variant TypeOTHER complex substitution
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3520752
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14336052
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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