A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619840



Internal ID6660026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17340313..17351655hg38UCSC Ensembl
Innerchr9:17340335..17351634hg38UCSC Ensembl
Outerchr9:17340292..17351677hg38UCSC Ensembl
chr9:17340311..17351653hg19UCSC Ensembl
Innerchr9:17340333..17351632hg19UCSC Ensembl
Outerchr9:17340290..17351675hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3811343
hg1911343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13412111, essv13412110
SamplesHG04014, HG03949
Known GenesCNTLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619840
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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