A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915272



Internal ID22690490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47493828..47495189hg38UCSC Ensembl
chr7:47533426..47534787hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg381362
hg191362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448210
Samples
Known GenesTNS3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915272
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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