A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988400



Internal ID20555440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13071142..13083143hg38UCSC Ensembl
chr11:13092689..13104690hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3812002
hg1912002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988400
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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