A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004788



Internal ID19094005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29013..121227hg38UCSC Ensembl
Innerchr4:29013..121107hg19UCSC Ensembl
Innerchr4:19013..111107hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3892215
hg1992095
hg1892095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5064n100
Supporting Variantsnssv3615255
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)nsv1004788
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer