A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3520752



Internal ID22390161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91481359..91508180hg38UCSC Ensembl
chr7:91110674..91137495hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3826822
hg1926822
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14336053, nssv14336051, nssv14336052, nssv14336054, nssv14336050
SamplesHG00512, NA19239, HG00731, HG00733, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3520752
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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