A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948227



Internal ID21368296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42021918..42022102hg38UCSC Ensembl
chr4:42023935..42024119hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196123
SamplesHG002
Known GenesSLC30A9
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948227
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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