A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641129



Internal ID7027903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69334109..69338971hg38UCSC Ensembl
Innerchr17:69334143..69338938hg38UCSC Ensembl
Outerchr17:69334076..69339005hg38UCSC Ensembl
chr17:67330250..67335112hg19UCSC Ensembl
Innerchr17:67330284..67335079hg19UCSC Ensembl
Outerchr17:67330217..67335146hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg384863
hg194863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15730614, essv15730612, essv15730616, essv15730615, essv15730613
SamplesHG02491, HG04162, HG03779, HG03703, HG04140
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641129
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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