A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994832



Internal ID20561872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90498444..90645732hg38UCSC Ensembl
chr11:90231612..90378900hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38147289
hg19147289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475257
Supporting Variants
Samples
Known GenesDISC1FP1, MIR4490
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994832
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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