A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041426



Internal ID19130645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:37620204..38044017hg38UCSC Ensembl
Innerchr12:38014006..38437819hg19UCSC Ensembl
Innerchr12:36300273..36724086hg18UCSC Ensembl
Cytoband12q11
Allele length
AssemblyAllele length
hg38423814
hg19423814
hg18423814
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1470n100
Supporting Variantsnssv3522908
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)nsv1041426
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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