A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029152



Internal ID19118371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:84380324..84440425hg38UCSC Ensembl
Innerchr8:85292559..85352660hg19UCSC Ensembl
Innerchr8:85455114..85515215hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3860102
hg1960102
hg1860102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7254n100
Supporting Variantsnssv3689639
Samples
Known GenesRALYL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029152
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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