A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6269161



Internal ID9246564
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 Flag1
Merged StatusS
Merged Variantsesv2664707
Supporting Variants
SamplesNA19720
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6269161
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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