A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026646



Internal ID18769178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:86099478..86165139hg38UCSC Ensembl
Innerchr8:87111707..87177368hg19UCSC Ensembl
Innerchr8:87180823..87246484hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3865662
hg1965662
hg1865662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7262n100
Supporting Variantsnssv3689673
Samples
Known GenesATP6V0D2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026646
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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