A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047600



Internal ID19136819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:48533731..48560442hg38UCSC Ensembl
Innerchr12:48927514..48954225hg19UCSC Ensembl
Innerchr12:47213781..47240492hg18UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3826712
hg1926712
hg1826712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1495n100
Supporting Variantsnssv3523522
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)nsv1047600
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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