A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620354



Internal ID7007225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34267077..34282789hg38UCSC Ensembl
Innerchr9:34267127..34282739hg38UCSC Ensembl
Outerchr9:34267015..34282851hg38UCSC Ensembl
chr9:34267075..34282787hg19UCSC Ensembl
Innerchr9:34267125..34282737hg19UCSC Ensembl
Outerchr9:34267013..34282849hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3815713
hg1915713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13458103
SamplesNA18602
Known GenesKIF24
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620354
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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