A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705136



Internal ID21377412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61496209..61501821hg38UCSC Ensembl
chr11:61263681..61269293hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg385613
hg195613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389861
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705136
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0287356


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