A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575626



Internal ID21524056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77869831..77869929hg38UCSC Ensembl
chr1:78335516..78335614hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066440
SamplesHG02011
Known GenesFAM73A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575626
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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