A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640760



Internal ID7027534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51031412..51032320hg38UCSC Ensembl
Innerchr17:51031462..51032270hg38UCSC Ensembl
Outerchr17:51031314..51032418hg38UCSC Ensembl
chr17:49108773..49109681hg19UCSC Ensembl
Innerchr17:49108823..49109631hg19UCSC Ensembl
Outerchr17:49108675..49109779hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38909
hg19909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15695681
SamplesHG00445
Known GenesSPAG9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640760
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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