A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665096



Internal ID9584515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:212699..337904hg38UCSC Ensembl
chr4:206488..331693hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38125206
hg19125206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv914e199
Supporting Variantsessv5426967
SamplesNA19713
Known GenesZNF141, ZNF732, ZNF876P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665096
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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