A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14366725



Internal ID22323259
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208858
Supporting Variants
SamplesNA19240
Known GenesZCCHC11
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14366725
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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