A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426259



Internal ID21083812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39967801..39971000hg38UCSC Ensembl
chr8:39825320..39828519hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167984
Samples
Known GenesIDO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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