A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519336



Internal ID18817617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:16010011..16051797hg38UCSC Ensembl
Innerchr12:16162945..16204731hg19UCSC Ensembl
Innerchr12:16054212..16095998hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3841787
hg1941787
hg1841787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050055
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)nssv3519336
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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