A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621008



Internal ID7007878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88515657..88519130hg38UCSC Ensembl
Innerchr9:88515660..88519128hg38UCSC Ensembl
Outerchr9:88515655..88519133hg38UCSC Ensembl
chr9:91130572..91134045hg19UCSC Ensembl
Innerchr9:91130575..91134043hg19UCSC Ensembl
Outerchr9:91130570..91134048hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg383474
hg193474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13549371, essv13549374, essv13549373, essv13549372, essv13549370
SamplesHG03130, NA19678, NA20355, HG02772, NA20334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621008
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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