A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454789



Internal ID21112342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35681266..35726797hg38UCSC Ensembl
chr9:35681263..35726794hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3845532
hg1945532
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220717
Samples
Known GenesMIR6852, TLN1, TPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454789
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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