A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569742



Internal ID21518104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119620899..119620970hg38UCSC Ensembl
chr1:120163522..120163593hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060171
SamplesHG02011
Known GenesZNF697
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569742
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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