A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600743



Internal ID21549384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67609495..67609554hg38UCSC Ensembl
chr15:67901833..67901892hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085384
SamplesNA19238
Known GenesMAP2K5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600743
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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