A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194190



Internal ID20761230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37166064..37167735hg38UCSC Ensembl
chr9:37166061..37167732hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg381672
hg191672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436014
Supporting Variants
Samples
Known GenesZCCHC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194190
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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