A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575609



Internal ID21524039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:81734332..81735088hg38UCSC Ensembl
chr1:82200017..82200773hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067275
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575609
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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