A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428794



Internal ID21086347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39608725..39609415hg38UCSC Ensembl
chr8:39466244..39466934hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169669
Samples
Known GenesADAM18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428794
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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