A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418566



Internal ID21076119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133866014..134670280hg38UCSC Ensembl
chr8:134878257..135682523hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38804267
hg19804267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164702
Samples
Known GenesZFAT, ZFAT-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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