A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012570



Internal ID21921913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73037640..73037698hg38UCSC Ensembl
chr8:73949875..73949933hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597020
Samples
Known GenesTERF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012570
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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