A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664707



Internal ID9584126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21651521..22713141hg38UCSC Ensembl
Outerchr17:21651521..22713176hg38UCSC Ensembl
Innerchr17:21554394..22212468hg19UCSC Ensembl
Outerchr17:21554360..22212503hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381061656
hg19658144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv539e199
Supporting Variantsessv6269161
SamplesNA19720
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664707
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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