A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449537



Internal ID21107090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34103197..34805619hg38UCSC Ensembl
chr9:34103195..34805616hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38702423
hg19702422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223736
Samples
Known GenesARID3C, C9orf24, CCL19, CCL21, CCL27, CNTFR, CNTFR-AS1, DCAF12, DCTN3, DNAI1, ENHO, FAM205A, FAM219A, GALT, IL11RA, KIAA1161, KIF24, NUDT2, RPP25L, SIGMAR1, UBAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449537
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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