A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573770



Internal ID21522178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46074085..46075925hg38UCSC Ensembl
chr7:46113683..46115523hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg381841
hg191841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151673
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573770
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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