A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436843



Internal ID21094396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136726294..136738847hg38UCSC Ensembl
chr9:139620746..139633299hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3812554
hg1912554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218110
Samples
Known GenesLCN10, SNHG7, SNORA17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436843
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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