A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432900



Internal ID21090453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73000657..73012497hg38UCSC Ensembl
chr8:73912892..73924732hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3811841
hg1911841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170351
Samples
Known GenesTERF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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