A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448776



Internal ID21106329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136577591..136723408hg38UCSC Ensembl
chr9:139472043..139617860hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38145818
hg19145818
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221996
Samples
Known GenesAGPAT2, EGFL7, FAM69B, MIR126
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448776
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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