A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446224



Internal ID21103777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71206261..71879773hg38UCSC Ensembl
chr9:73821177..74494689hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38673513
hg19673513
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7819n223
Supporting Variantsnssv18226158
Samples
Known GenesABHD17B, TMEM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446224
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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