A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565954



Internal ID21514272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156658538..156666749hg38UCSC Ensembl
chr5:156085549..156093760hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg388212
hg198212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130472
SamplesHG03486
Known GenesSGCD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565954
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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