A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432502



Internal ID21090055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4659501..4669900hg38UCSC Ensembl
chr9:4659501..4669900hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234260
Samples
Known GenesPPAPDC2, SPATA6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432502
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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