A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641288



Internal ID7028062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76433728..76443973hg38UCSC Ensembl
Innerchr17:76433767..76443934hg38UCSC Ensembl
Outerchr17:76433689..76444012hg38UCSC Ensembl
chr17:74429810..74440055hg19UCSC Ensembl
Innerchr17:74429849..74440016hg19UCSC Ensembl
Outerchr17:74429771..74440094hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3810246
hg1910246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15744092
SamplesHG02040
Known GenesUBE2O
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641288
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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