A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177908



Internal ID20744948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5736213..5736730hg38UCSC Ensembl
chr9:5736213..5736730hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434583
Supporting Variants
Samples
Known GenesKIAA1432
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177908
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00056


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