A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431209



Internal ID21088762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26093283..26129476hg38UCSC Ensembl
chr9:26093281..26129474hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3836194
hg1936194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194371
Samples
Known GenesLOC100506422
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431209
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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