A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050523



Internal ID18793054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:109343610..109384054hg38UCSC Ensembl
Innerchr12:109781415..109821859hg19UCSC Ensembl
Innerchr12:108265798..108306242hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3840445
hg1940445
hg1840445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1555n100
Supporting Variantsnssv3524899
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)nsv1050523
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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