A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13628802



Internal ID3630618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129764130..129768243hg38UCSC Ensembl
Innerchr9:129764130..129768243hg38UCSC Ensembl
Outerchr9:129763828..129768578hg38UCSC Ensembl
chr9:132526409..132530522hg19UCSC Ensembl
Innerchr9:132526409..132530522hg19UCSC Ensembl
Outerchr9:132526107..132530857hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384114
hg194114
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621844
Supporting Variants
SamplesNA18915
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13628802
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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