A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621163



Internal ID7008032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96349651..96353440hg38UCSC Ensembl
Innerchr9:96349651..96353440hg38UCSC Ensembl
Outerchr9:96349413..96353691hg38UCSC Ensembl
chr9:99111933..99115722hg19UCSC Ensembl
Innerchr9:99111933..99115722hg19UCSC Ensembl
Outerchr9:99111695..99115973hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg383790
hg193790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13572585
SamplesHG01868
Known GenesSLC35D2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621163
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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