A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441497



Internal ID21099050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104874701..104875400hg38UCSC Ensembl
chr9:107636982..107637681hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173312
Samples
Known GenesABCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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