A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449895



Internal ID21107448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35661373..35662982hg38UCSC Ensembl
chr9:35661370..35662979hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381610
hg191610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192628
Samples
Known GenesARHGEF39, CCDC107
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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