A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429577



Internal ID21087130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37888119..37890076hg38UCSC Ensembl
chr8:37745637..37747594hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg381958
hg191958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168909
Samples
Known GenesRAB11FIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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