A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621359



Internal ID7008228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105610038..105611160hg38UCSC Ensembl
Innerchr9:105610038..105611160hg38UCSC Ensembl
Outerchr9:105609759..105611322hg38UCSC Ensembl
chr9:108372319..108373441hg19UCSC Ensembl
Innerchr9:108372319..108373441hg19UCSC Ensembl
Outerchr9:108372040..108373603hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381123
hg191123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13593257, essv13593255, essv13593250, essv13593258, essv13593249, essv13593251, essv13593253, essv13593252, essv13593254, essv13593259, essv13593256
SamplesHG02610, NA18881, HG02419, NA19092, HG02769, NA18519, NA19225, HG02772, HG03461, NA19900, HG02051
Known GenesFKTN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621359
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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