A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526129



Internal ID18824410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:126155998..126320609hg38UCSC Ensembl
Innerchr12:126640544..126805155hg19UCSC Ensembl
Innerchr12:125206497..125371108hg18UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38164612
hg19164612
hg18164612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049051
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3526129
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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