A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581715



Internal ID21530219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2759047..2760773hg38UCSC Ensembl
chr1:2629535..2631261hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg381727
hg191727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064510
SamplesHG03486
Known GenesTTC34
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581715
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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