A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439929



Internal ID21097482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131110891..131115179hg38UCSC Ensembl
chr9:133986278..133990566hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg384289
hg194289
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219224
Samples
Known GenesAIF1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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