A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427962



Internal ID21085515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6865285..6874461hg38UCSC Ensembl
chr9:6865285..6874461hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg389177
hg199177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186105
Samples
Known GenesKDM4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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