A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676591



Internal ID9596010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21651521..22710477hg38UCSC Ensembl
chr17:21551635..22209804hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381058957
hg19658170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv539e199
Supporting Variantsessv6373294, essv6557500
SamplesHG00476, HG01082
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676591
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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