A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6238330



Internal ID9728197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183495794..183496921hg38UCSC Ensembl
chr4:184416947..184418074hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381128
hg191128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665622
Supporting Variants
SamplesNA19652
Known GenesLOC389247
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6238330
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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