A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051012



Internal ID19140231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:21577302..21628207hg38UCSC Ensembl
Innerchr12:21730236..21781141hg19UCSC Ensembl
Innerchr12:21621503..21672408hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3850906
hg1950906
hg1850906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513469
Samples
Known GenesGYS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051012
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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