A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424669



Internal ID21082222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41436577..41517177hg38UCSC Ensembl
chr8:41294096..41374696hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3880601
hg1980601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166898
Samples
Known GenesGOLGA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424669
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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