A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660405



Internal ID21608710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:116853..116853hg38UCSC Ensembl
chr11:179813..179813hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg385451
hg195451
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098236, nssv17085132, nssv17088168
SamplesHG00096, HG00512, HG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660405
Frequency
Sample Size35
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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