A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637112



Internal ID21585417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84345108..84345108hg38UCSC Ensembl
chr6:85054826..85054826hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149351
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637112
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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