A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171537



Internal ID20738577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100172931..100182818hg38UCSC Ensembl
chr9:102935213..102945100hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg389888
hg199888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436470
Supporting Variants
Samples
Known GenesINVS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171537
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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