A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065494



Internal ID21457577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3906468..3906468hg38UCSC Ensembl
chr1:3823032..3823032hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg385647
hg195647
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605557
Supporting Variants
SamplesHG02587
Known GenesLINC01134
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065494
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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