A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428608



Internal ID21086161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36670743..36758942hg38UCSC Ensembl
chr8:36528261..36616460hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3888200
hg1988200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167494
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428608
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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