A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171552



Internal ID20738592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100453363..100453752hg38UCSC Ensembl
chr9:103215645..103216034hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446642
Supporting Variants
Samples
Known GenesMSANTD3-TMEFF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171552
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00012


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