A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429331



Internal ID21086884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7062594..7087747hg38UCSC Ensembl
chr9:7062594..7087747hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3825154
hg1925154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196755
Samples
Known GenesKDM4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429331
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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