A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012668



Internal ID19101885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..121670hg38UCSC Ensembl
Innerchr4:12269..121550hg19UCSC Ensembl
Innerchr4:2269..111550hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38109402
hg19109282
hg18109282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5059n100
Supporting Variantsnssv3615208, nssv3738050, nssv3615213, nssv3738048, nssv3738047, nssv3615211, nssv3615210, nssv3738049, nssv3615209, nssv3738045, nssv3738044, nssv3738046, nssv3615212, nssv3615207
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012668
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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