A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038689



Internal ID19127908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:66780650..66863655hg38UCSC Ensembl
Innerchr12:67174430..67257435hg19UCSC Ensembl
Innerchr12:65460697..65543702hg18UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3883006
hg1983006
hg1883006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1522n100
Supporting Variantsnssv3524597
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)nsv1038689
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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