A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429324



Internal ID21086877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138615839..138616146hg38UCSC Ensembl
chr8:139628082..139628389hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166465
Samples
Known GenesCOL22A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429324
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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