A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572500



Internal ID21520891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168297332..168297381hg38UCSC Ensembl
chr4:169218483..169218532hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129515
SamplesHG02492
Known GenesDDX60
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572500
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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