A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427070



Internal ID21084623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74825901..74829100hg38UCSC Ensembl
chr8:75738136..75741335hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170138
Samples
Known GenesPI15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427070
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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