A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004818



Internal ID18747349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16688..59167hg38UCSC Ensembl
Innerchr4:16688..59060hg19UCSC Ensembl
Innerchr4:6688..49060hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3842480
hg1942373
hg1842373
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5061n100
Supporting Variantsnssv3615233
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)nsv1004818
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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