A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034957



Internal ID18777489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:96386..460640hg38UCSC Ensembl
Innerchr8:46386..410640hg19UCSC Ensembl
Innerchr8:36386..400640hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38364255
hg19364255
hg18364255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6789n100
Supporting Variantsnssv3674907, nssv3674906, nssv3674908, nssv3674905
Samples
Known GenesFAM87A, FBXO25, OR4F21, RPL23AP53, ZNF596
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034957
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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