A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613253



Internal ID20986324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18585051..19023375hg38UCSC Ensembl
chr7:18624674..19062998hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38438325
hg19438325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231805
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613253
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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