A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419730



Internal ID21077283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39743101..39744100hg38UCSC Ensembl
chr8:39600620..39601619hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169684
Samples
Known GenesADAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419730
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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