A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933521



Internal ID21353590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100922995..100923315hg38UCSC Ensembl
chr1:101388551..101388871hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15176460
SamplesHG002
Known GenesSLC30A7
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933521
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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