A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186830



Internal ID20753870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30640986..30737179hg38UCSC Ensembl
chr9:30640984..30737177hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3896194
hg1996194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428340
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186830
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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