A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043439



Internal ID19132658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:83219138..83277947hg38UCSC Ensembl
Innerchr12:83612917..83671726hg19UCSC Ensembl
Innerchr12:82137048..82195857hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3858810
hg1958810
hg1858810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1534n100
Supporting Variantsnssv3524724
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043439
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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