A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034988



Internal ID18777519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10734291..10946733hg38UCSC Ensembl
Innerchr8:10591801..10804243hg19UCSC Ensembl
Innerchr8:10629211..10841653hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38212443
hg19212443
hg18212443
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7011n100
Supporting Variantsnssv3681725
Samples
Known GenesMIR1322, PINX1, XKR6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034988
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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