A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621081



Internal ID6661262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92476575..92537444hg38UCSC Ensembl
Innerchr9:92476575..92537444hg38UCSC Ensembl
Outerchr9:92476075..92537944hg38UCSC Ensembl
chr9:95238857..95299726hg19UCSC Ensembl
Innerchr9:95238857..95299726hg19UCSC Ensembl
Outerchr9:95238357..95300226hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3860870
hg1960870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559432, essv13559431
SamplesNA20507, HG02820
Known GenesASPN, CENPP, ECM2, MIR4670
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621081
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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