A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415971



Internal ID21073524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62899701..62927700hg38UCSC Ensembl
chr8:63812260..63840259hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3828000
hg1928000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169779
Samples
Known GenesNKAIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415971
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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