A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044455



Internal ID19133674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:16010011..16049757hg38UCSC Ensembl
Innerchr12:16162945..16202691hg19UCSC Ensembl
Innerchr12:16054212..16093958hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3839747
hg1939747
hg1839747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1395n100
Supporting Variantsnssv3516150
Samples
Known GenesDERA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044455
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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