A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420081



Internal ID21077634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70700350..70740618hg38UCSC Ensembl
chr8:71612585..71652853hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3840269
hg1940269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169565
Samples
Known GenesXKR9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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