A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446731



Internal ID21104284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34707347..34711428hg38UCSC Ensembl
chr9:34707344..34711425hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg384082
hg194082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182236
Samples
Known GenesCCL21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446731
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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