A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657755



Internal ID9923860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8692726..8692876hg38UCSC Ensembl
Outerchr17:8692689..8692926hg38UCSC Ensembl
Innerchr17:8596044..8596194hg19UCSC Ensembl
Outerchr17:8596007..8596244hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv533e199
Supporting Variantsessv6245304, essv6187493, essv5843323, essv5802845, essv5793012, essv6531122, essv6275059, essv5520109, essv6194010, essv6054991, essv5633576, essv5442092, essv6543449, essv5465726, essv6223941, essv6194717, essv6120882, essv6536784
SamplesNA19394, HG00542, NA19397, NA18924, NA18596, HG00127, HG01350, NA19379, HG00683, NA19371, NA19731, NA20299, NA12829, HG01101, HG01204, NA19428, NA19759, NA18620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657755
Frequency
Sample Size1151
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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