A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029213



Internal ID19118432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88828949..88939682hg38UCSC Ensembl
Innerchr8:89841178..89951911hg19UCSC Ensembl
Innerchr8:89910294..90021027hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38110734
hg19110734
hg18110734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7266n100
Supporting Variantsnssv3689695
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)nsv1029213
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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