A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065095



Internal ID21455885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28377127..28381202hg38UCSC Ensembl
chr1:28703638..28707713hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg384076
hg194076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569662
Supporting Variants
SamplesHG02492
Known GenesPHACTR4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065095
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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