A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433429



Internal ID21090982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:130302513..130305777hg38UCSC Ensembl
chr8:131314759..131318023hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg383265
hg193265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165075
Samples
Known GenesASAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433429
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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