A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415861



Internal ID21073414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:71880560..71897134hg38UCSC Ensembl
chr8:72792795..72809369hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3816575
hg1916575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169654
Samples
Known GenesLOC100132891
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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