A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528819



Internal ID22398210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81080270..81080456hg38UCSC Ensembl
chr7:80709586..80709772hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14335093
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528819
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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