A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424048



Internal ID21081601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53668501..53682000hg38UCSC Ensembl
chr8:54581061..54594560hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3813500
hg1913500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424048
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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