A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6437151



Internal ID9316594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165045815..165046589hg38UCSC Ensembl
chr4:165966967..165967741hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664937
Supporting Variants
SamplesNA18507
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6437151
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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