A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639018



Internal ID21587323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111091667..111091667hg38UCSC Ensembl
chr6:111412870..111412870hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144575
SamplesHG02818
Known GenesSLC16A10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639018
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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