A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419895



Internal ID21077448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24324892..24351031hg38UCSC Ensembl
chr8:24182405..24208544hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3826140
hg1926140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167201
Samples
Known GenesADAM28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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