A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565461



Internal ID21513774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156717803..156718933hg38UCSC Ensembl
chr5:156144814..156145944hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125746
SamplesHG03125
Known GenesSGCD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565461
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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