A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029820



Internal ID19119039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:80559891..80584622hg38UCSC Ensembl
Innerchr5:79855710..79880441hg19UCSC Ensembl
Innerchr5:79891466..79916197hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3824732
hg1924732
hg1824732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5707n100
Supporting Variantsnssv3639129, nssv3639131, nssv3639122, nssv3639127, nssv3639125, nssv3639130, nssv3639121, nssv3639124, nssv3639126, nssv3639123, nssv3639128
Samples
Known GenesANKRD34B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029820
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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