A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621070



Internal ID6661251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91776697..91777673hg38UCSC Ensembl
Innerchr9:91776697..91777673hg38UCSC Ensembl
Outerchr9:91776479..91777879hg38UCSC Ensembl
chr9:94538979..94539955hg19UCSC Ensembl
Innerchr9:94538979..94539955hg19UCSC Ensembl
Outerchr9:94538761..94540161hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38977
hg19977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559244
SamplesHG01101
Known GenesROR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621070
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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