A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639853



Internal ID7026631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6968231..6973869hg38UCSC Ensembl
Innerchr17:6968235..6973865hg38UCSC Ensembl
Outerchr17:6968227..6973873hg38UCSC Ensembl
chr17:6871550..6877188hg19UCSC Ensembl
Innerchr17:6871554..6877184hg19UCSC Ensembl
Outerchr17:6871546..6877192hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg385639
hg195639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15602850, essv15602854, essv15602855, essv15602856, essv15602857, essv15602852, essv15602849, essv15602862, essv15602858, essv15602853, essv15602861, essv15602851, essv15602859, essv15602863, essv15602860
SamplesHG03247, NA20298, NA18510, HG02620, NA19238, HG03195, HG03267, NA19437, HG03451, HG03539, HG03117, HG02837, HG02982, HG03313, HG02013
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639853
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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