A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012779



Internal ID19101996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:80531712..80563946hg38UCSC Ensembl
Innerchr3:80580862..80613096hg19UCSC Ensembl
Innerchr3:80663552..80695786hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3832235
hg1932235
hg1832235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4799n100
Supporting Variantsnssv3596235
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)nsv1012779
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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