A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014656



Internal ID18757191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29013..69821hg38UCSC Ensembl
Innerchr4:29013..69713hg19UCSC Ensembl
Innerchr4:19013..59713hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3840809
hg1940701
hg1840701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5061n100
Supporting Variantsnssv3615252
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)nsv1014656
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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