A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621344



Internal ID6661523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104767944..104773111hg38UCSC Ensembl
Innerchr9:104767944..104773111hg38UCSC Ensembl
Outerchr9:104767632..104773259hg38UCSC Ensembl
chr9:107530225..107535392hg19UCSC Ensembl
Innerchr9:107530225..107535392hg19UCSC Ensembl
Outerchr9:107529913..107535540hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385168
hg195168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13591918, essv13591919
SamplesNA19794, NA11893
Known GenesNIPSNAP3B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621344
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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