A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641338



Internal ID7028112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78646138..78649187hg38UCSC Ensembl
Innerchr17:78646638..78648687hg38UCSC Ensembl
Outerchr17:78645138..78650187hg38UCSC Ensembl
chr17:76642220..76645269hg19UCSC Ensembl
Innerchr17:76642720..76644769hg19UCSC Ensembl
Outerchr17:76641220..76646269hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg383050
hg193050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15753144
SamplesHG01992
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641338
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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