A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419510



Internal ID21077063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39359801..39578400hg38UCSC Ensembl
chr8:39217320..39435919hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38218600
hg19218600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7318n223
Supporting Variantsnssv18169030
Samples
Known GenesADAM3A, ADAM5, LOC100130964
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419510
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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