A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621871



Internal ID7008737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130909668..130917508hg38UCSC Ensembl
Innerchr9:130910168..130917008hg38UCSC Ensembl
Outerchr9:130908668..130918508hg38UCSC Ensembl
chr9:133785055..133792895hg19UCSC Ensembl
Innerchr9:133785555..133792395hg19UCSC Ensembl
Outerchr9:133784055..133793895hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg387841
hg197841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13630761, essv13630762
SamplesHG04212, NA19003
Known GenesFIBCD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621871
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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