A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449069



Internal ID21106622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96260811..96265158hg38UCSC Ensembl
chr9:99023093..99027440hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg384348
hg194348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178762
Samples
Known GenesHSD17B3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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