A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217676



Internal ID20784716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6515201..6813500hg38UCSC Ensembl
chr9:6515201..6813500hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38298300
hg19298300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431609
Supporting Variants
Samples
Known GenesGLDC, KDM4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217676
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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