A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557281



Internal ID16344690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7835165..7963425hg38UCSC Ensembl
Innerchr12:7987761..8116021hg19UCSC Ensembl
Innerchr12:7879028..8007288hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38128261
hg19128261
hg18128261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2329n54
Supporting Variantsnssv787276
Samples
Known GenesSLC2A14, SLC2A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557281
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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