A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137752



Internal ID21464360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52464993..52465712hg38UCSC Ensembl
chr4:53331159..53331878hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582852
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137752
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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