A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066441



Internal ID21462297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77870139..77870268hg38UCSC Ensembl
chr1:78335824..78335953hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579743
Supporting Variants
SamplesHG02818
Known GenesFAM73A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066441
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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