A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445300



Internal ID21102853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116596324..116608603hg38UCSC Ensembl
chr9:119358603..119370882hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3812280
hg1912280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174145
Samples
Known GenesASTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445300
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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