A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641318



Internal ID7028092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77645325..77655199hg38UCSC Ensembl
Innerchr17:77645349..77655176hg38UCSC Ensembl
Outerchr17:77645302..77655223hg38UCSC Ensembl
chr17:75641407..75651281hg19UCSC Ensembl
Innerchr17:75641431..75651258hg19UCSC Ensembl
Outerchr17:75641384..75651305hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg389875
hg199875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15748497, essv15748494, essv15748496, essv15748495
SamplesNA12286, HG03911, HG01605, HG00128
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641318
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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