A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637356



Internal ID21585661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15103239..15103239hg38UCSC Ensembl
chr6:15103470..15103470hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148542
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637356
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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