A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569655



Internal ID21518016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129214931..129216102hg38UCSC Ensembl
chr7:128854772..128855943hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg381172
hg191172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153387
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569655
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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