A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583271



Internal ID21531794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2789118..2789431hg38UCSC Ensembl
chr7:2828752..2829065hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154363
SamplesHG02818
Known GenesGNA12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583271
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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