A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993395



Internal ID20560436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56900170..56964294hg38UCSC Ensembl
chr11:56667646..56731769hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3864125
hg1964124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466008
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993395
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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