A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042425



Internal ID19131644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:12366385..12387521hg38UCSC Ensembl
Innerchr12:12519319..12540455hg19UCSC Ensembl
Innerchr12:12410586..12431722hg18UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3821137
hg1921137
hg1821137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1392n100
Supporting Variantsnssv3516266, nssv3515369
Samples
Known GenesLOH12CR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042425
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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