A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5061n100



Internal ID20156677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16688..69821hg38UCSC Ensembl
chr4:16688..69713hg19UCSC Ensembl
chr4:6688..59713hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3853134
hg1953026
hg1853026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004818, nsv1002737, nsv1014489, nsv998790, nsv1006971, nsv1014656
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)dgv5061n100
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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