A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436470



Internal ID21094023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100172931..100182818hg38UCSC Ensembl
chr9:102935213..102945100hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg389888
hg199888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171537
Samples
Known GenesINVS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436470
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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