A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026102



Internal ID19115319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101375798..101388365hg38UCSC Ensembl
Innerchr8:102388026..102400593hg19UCSC Ensembl
Innerchr8:102457202..102469769hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3812568
hg1912568
hg1812568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7277n100
Supporting Variantsnssv3689753, nssv3689754, nssv3689752, nssv3689755
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)nsv1026102
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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