A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13618977



Internal ID6319232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125393126..125399969hg38UCSC Ensembl
Innerchr9:125393143..125399953hg38UCSC Ensembl
Outerchr9:125393110..125399986hg38UCSC Ensembl
chr9:128155405..128162248hg19UCSC Ensembl
Innerchr9:128155422..128162232hg19UCSC Ensembl
Outerchr9:128155389..128162265hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg386844
hg196844
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621745
Supporting Variants
SamplesNA19917
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13618977
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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