A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639697



Internal ID7026475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1703507..1704786hg38UCSC Ensembl
Innerchr17:1703558..1704735hg38UCSC Ensembl
Outerchr17:1703456..1704837hg38UCSC Ensembl
chr17:1606801..1608080hg19UCSC Ensembl
Innerchr17:1606852..1608029hg19UCSC Ensembl
Outerchr17:1606750..1608131hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381280
hg191280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15581610
SamplesHG03884
Known GenesTLCD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639697
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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