A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442529



Internal ID21100082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101418745..101443576hg38UCSC Ensembl
chr9:104181027..104205858hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3824832
hg1924832
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218645
Samples
Known GenesALDOB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442529
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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