A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573698



Internal ID21522106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8906451..8906761hg38UCSC Ensembl
chr1:8966510..8966820hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067297
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573698
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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