A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677663



Internal ID21199520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190965997..190966134hg38UCSC Ensembl
chr3:190683786..190683923hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807877
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677663
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.09375


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