A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567360



Internal ID21515695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155594420..155594488hg38UCSC Ensembl
chr7:155387114..155387182hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153055
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567360
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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