A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817574



Internal ID21262912
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 StatusM
Merged Variants
Supporting Variantsnssv13700297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817574
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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