A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621004



Internal ID7007874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88405258..88414567hg38UCSC Ensembl
Innerchr9:88405270..88414555hg38UCSC Ensembl
Outerchr9:88405246..88414579hg38UCSC Ensembl
chr9:91020173..91029482hg19UCSC Ensembl
Innerchr9:91020185..91029470hg19UCSC Ensembl
Outerchr9:91020161..91029494hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg389310
hg199310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13549135, essv13549136
SamplesNA19024, NA19360
Known GenesSPIN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621004
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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