A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1001e214



Internal ID22756895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57179132..57238292hg38UCSC Ensembl
chr4:58045298..58104458hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3859161
hg1959161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3600599, esv3600598
SamplesNA12414, HG01528, HG01170, HG01256, NA19663, HG01613, HG00256, HG01917
Known GenesIGFBP7-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1001e214
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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