A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6351261



Internal ID9328664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126631538..126632675hg38UCSC Ensembl
Outerchr9:126631501..126632725hg38UCSC Ensembl
Innerchr9:129393817..129394954hg19UCSC Ensembl
Outerchr9:129393780..129395004hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381225
hg191225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2659178
Supporting Variants
SamplesHG00737
Known GenesLMX1B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6351261
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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