A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424932



Internal ID21082485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11194001..11200600hg38UCSC Ensembl
chr8:11051510..11058109hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233358
Samples
Known GenesXKR6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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