A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619851



Internal ID7006725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17645643..17719781hg38UCSC Ensembl
Innerchr9:17645646..17719778hg38UCSC Ensembl
Outerchr9:17645640..17719784hg38UCSC Ensembl
chr9:17645641..17719779hg19UCSC Ensembl
Innerchr9:17645644..17719776hg19UCSC Ensembl
Outerchr9:17645638..17719782hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3874139
hg1974139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1458e214
Supporting Variantsessv13412196, essv13412197
SamplesNA20126, HG02107
Known GenesSH3GL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619851
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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