A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449573



Internal ID21107126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131088865..131090674hg38UCSC Ensembl
chr9:133964252..133966061hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg381810
hg191810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231557
Samples
Known GenesLAMC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449573
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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