A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516150



Internal ID18814431
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 StatusS
Merged Variantsnsv1044455
Supporting Variants
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)nssv3516150
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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