A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169590



Internal ID21313823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:129104450..129115872hg38UCSC Ensembl
Outerchr8:129099922..129124380hg38UCSC Ensembl
Innerchr8:130116696..130128118hg19UCSC Ensembl
Outerchr8:130112168..130136626hg19UCSC Ensembl
Innerchr8:130185878..130197300hg18UCSC Ensembl
Outerchr8:130181350..130205808hg18UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3824459
hg1924459
hg1824459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242280
SamplesMLY_9
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169590
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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