A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640183



Internal ID7026958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19811560..19815414hg38UCSC Ensembl
Innerchr17:19811560..19815414hg38UCSC Ensembl
Outerchr17:19811060..19815914hg38UCSC Ensembl
chr17:19714873..19718727hg19UCSC Ensembl
Innerchr17:19714873..19718727hg19UCSC Ensembl
Outerchr17:19714373..19719227hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383855
hg193855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15648054
SamplesNA19682
Known GenesULK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640183
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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