A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570086



Internal ID21518450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88385869..88385920hg38UCSC Ensembl
chr7:88015184..88015235hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149498
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570086
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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