A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621164



Internal ID7008033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96410090..96411831hg38UCSC Ensembl
Innerchr9:96410093..96411828hg38UCSC Ensembl
Outerchr9:96410087..96411834hg38UCSC Ensembl
chr9:99172372..99174113hg19UCSC Ensembl
Innerchr9:99172375..99174110hg19UCSC Ensembl
Outerchr9:99172369..99174116hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381742
hg191742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13572586
SamplesHG01784
Known GenesZNF367
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621164
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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