A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561706



Internal ID22430474
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 StatusM
Merged Variants
Supporting Variantsnssv14368991
SamplesNA19239
Known GenesC1orf87
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561706
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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