A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054898



Internal ID19144117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:63522127..63742865hg38UCSC Ensembl
Innerchr12:63915907..64136645hg19UCSC Ensembl
Innerchr12:62202174..62422912hg18UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg38220739
hg19220739
hg18220739
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1516n100
Supporting Variantsnssv3523672
Samples
Known GenesDPY19L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054898
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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