A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561626



Internal ID22430394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220844370..220844370hg38UCSC Ensembl
chr1:221017712..221017712hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14308589, nssv14308588
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561626
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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