A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435157



Internal ID21092710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19392779..19491739hg38UCSC Ensembl
chr9:19392777..19491737hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3898961
hg1998961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7639n223
Supporting Variantsnssv18234335
Samples
Known GenesACER2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435157
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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