A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428337



Internal ID21085890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28639480..28814968hg38UCSC Ensembl
chr9:28639478..28814966hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38175489
hg19175489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7673n223
Supporting Variantsnssv18195203
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428337
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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