A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064024



Internal ID19153243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10548565..10775598hg38UCSC Ensembl
Innerchr21:10736859..10963892hg19UCSC Ensembl
Innerchr21:9758730..9985763hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38227034
hg19227034
hg18227034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4351n100
Supporting Variantsnssv3583622
Samples
Known GenesTPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064024
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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