A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047762



Internal ID19136981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:12367972..12388935hg38UCSC Ensembl
Innerchr12:12520906..12541869hg19UCSC Ensembl
Innerchr12:12412173..12433136hg18UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3820964
hg1920964
hg1820964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1392n100
Supporting Variantsnssv3521415, nssv3516377
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)nsv1047762
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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