A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700297



Internal ID21222132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128118501..128118629hg38UCSC Ensembl
chr8:129130747..129130875hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817574
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700297
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.1


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