A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640443



Internal ID7027218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35193963..35229757hg38UCSC Ensembl
Innerchr17:35194013..35229707hg38UCSC Ensembl
Outerchr17:35193889..35229831hg38UCSC Ensembl
chr17:33520982..33556776hg19UCSC Ensembl
Innerchr17:33521032..33556726hg19UCSC Ensembl
Outerchr17:33520908..33556850hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3835795
hg1935795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15664508
SamplesHG02461
Known GenesSLC35G3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640443
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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