A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585208



Internal ID6972732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10936329..10945192hg38UCSC Ensembl
Innerchr1:10936829..10944692hg38UCSC Ensembl
Outerchr1:10935329..10946192hg38UCSC Ensembl
chr1:10996386..11005249hg19UCSC Ensembl
Innerchr1:10996886..11004749hg19UCSC Ensembl
Outerchr1:10995386..11006249hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg388864
hg198864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9853352
SamplesHG01967
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585208
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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