A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620400



Internal ID6660583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36569264..36574849hg38UCSC Ensembl
Innerchr9:36569321..36574792hg38UCSC Ensembl
Outerchr9:36569207..36574906hg38UCSC Ensembl
chr9:36569261..36574846hg19UCSC Ensembl
Innerchr9:36569318..36574789hg19UCSC Ensembl
Outerchr9:36569204..36574903hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg385586
hg195586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13462843
SamplesNA21133
Known GenesMELK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620400
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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