A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208858



Internal ID22357027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52428570..52429136hg38UCSC Ensembl
chr1:52894242..52894808hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14366725
SamplesNA19240
Known GenesZCCHC11
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208858
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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