A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453152



Internal ID21110705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136200993..136256057hg38UCSC Ensembl
chr9:139092839..139147903hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3855065
hg1955065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7959n223
Supporting Variantsnssv18231751
Samples
Known GenesLHX3, QSOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453152
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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