A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13633399



Internal ID5700690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132039990..132045700hg38UCSC Ensembl
Innerchr9:132039990..132045700hg38UCSC Ensembl
Outerchr9:132039733..132045930hg38UCSC Ensembl
chr9:134915377..134921087hg19UCSC Ensembl
Innerchr9:134915377..134921087hg19UCSC Ensembl
Outerchr9:134915120..134921317hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg385711
hg195711
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621907
Supporting Variants
SamplesNA19089
Known GenesMED27
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13633399
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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