A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025424



Internal ID19114642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114615344..114638558hg38UCSC Ensembl
Innerchr8:115627573..115650787hg19UCSC Ensembl
Innerchr8:115696749..115719963hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3823215
hg1923215
hg1823215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7295n100
Supporting Variantsnssv3691337
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025424
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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