A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5439177



Internal ID8416580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129764115..129768202hg38UCSC Ensembl
chr9:132526394..132530481hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384088
hg194088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662571
Supporting Variants
SamplesNA18908
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5439177
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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