A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6584106



Internal ID9909448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99997428..99998160hg38UCSC Ensembl
chr4:100918585..100919317hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663322
Supporting Variants
SamplesNA20805
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6584106
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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