A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177871



Internal ID20744911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99906553..99908251hg38UCSC Ensembl
chr9:102668835..102670533hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381699
hg191699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449703
Supporting Variants
Samples
Known GenesLOC441461, STX17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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