A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061057



Internal ID21432351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165761972..165762251hg38UCSC Ensembl
chr1:165731209..165731488hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584199
Supporting Variants
SamplesHG00731
Known GenesTMCO1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061057
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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