A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6591172



Internal ID9721321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128429546..128434056hg38UCSC Ensembl
Outerchr9:128429509..128434106hg38UCSC Ensembl
Innerchr9:131191825..131196335hg19UCSC Ensembl
Outerchr9:131191788..131196385hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384598
hg194598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665611
Supporting Variants
SamplesNA19472
Known GenesCERCAM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6591172
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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