A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431714



Internal ID21089267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24006221..24007050hg38UCSC Ensembl
chr8:23863734..23864563hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431714
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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