A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004066



Internal ID19093283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68672892..68698250hg38UCSC Ensembl
Innerchr3:68722043..68747401hg19UCSC Ensembl
Innerchr3:68804733..68830091hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3825359
hg1925359
hg1825359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4772n100
Supporting Variantsnssv3594148, nssv3594147
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)nsv1004066
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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