A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453482



Internal ID21111035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137184214..137189201hg38UCSC Ensembl
chr9:140078666..140083653hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg384988
hg194988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234018
Samples
Known GenesANAPC2, SSNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453482
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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