A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13412111



Internal ID3413927
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619840
Supporting Variants
SamplesHG04014
Known GenesCNTLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13412111
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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