A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580778



Internal ID21529272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:118282841..118282934hg38UCSC Ensembl
chr5:117618536..117618629hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134804
SamplesNA12878
Known GenesLOC100505811
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580778
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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