A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640909



Internal ID6680994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59695262..59696664hg38UCSC Ensembl
Innerchr17:59695295..59696632hg38UCSC Ensembl
Outerchr17:59695230..59696697hg38UCSC Ensembl
chr17:57772623..57774025hg19UCSC Ensembl
Innerchr17:57772656..57773993hg19UCSC Ensembl
Outerchr17:57772591..57774058hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg381403
hg191403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15711838
SamplesHG01861
Known GenesCLTC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640909
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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