A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428424



Internal ID21085977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74705590..74706317hg38UCSC Ensembl
chr8:75617825..75618552hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170127
Samples
Known GenesFLJ39080, MIR2052
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428424
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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