A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416758



Internal ID21074311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64742626..64743497hg38UCSC Ensembl
chr8:65655183..65656054hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38872
hg19872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169472
Samples
Known GenesCYP7B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416758
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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