A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621145



Internal ID6661324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95115924..95121573hg38UCSC Ensembl
Innerchr9:95115925..95121572hg38UCSC Ensembl
Outerchr9:95115923..95121574hg38UCSC Ensembl
chr9:97878206..97883855hg19UCSC Ensembl
Innerchr9:97878207..97883854hg19UCSC Ensembl
Outerchr9:97878205..97883856hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385650
hg195650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13571769
SamplesHG02006
Known GenesFANCC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621145
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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