A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431938



Internal ID21089491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18176701..18177500hg38UCSC Ensembl
chr8:18034210..18035009hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166375
Samples
Known GenesNAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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