A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528765



Internal ID22398156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95074414..95074555hg38UCSC Ensembl
chr8:96086642..96086783hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342816
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528765
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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