A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065906



Internal ID21502642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60064774..60064774hg38UCSC Ensembl
chr1:60530446..60530446hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619145
Supporting Variants
SamplesNA19239
Known GenesC1orf87
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065906
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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