A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447100



Internal ID21104653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122832501..122945100hg38UCSC Ensembl
chr9:125594780..125707379hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38112600
hg19112600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234929
Samples
Known GenesRABGAP1, RC3H2, SNORD90, ZBTB26, ZBTB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447100
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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