A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529570



Internal ID22398961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40612215..40612864hg38UCSC Ensembl
chr8:40469734..40470383hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14341331
SamplesHG00732
Known GenesZMAT4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529570
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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