A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13710128



Internal ID21231900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42021920..42022103hg38UCSC Ensembl
chr4:42023937..42024120hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810972
Supporting Variants
Samples
Known GenesSLC30A9
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13710128
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.671875


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