A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640987



Internal ID7027761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63278471..63282919hg38UCSC Ensembl
Innerchr17:63278499..63282891hg38UCSC Ensembl
Outerchr17:63278443..63282947hg38UCSC Ensembl
chr17:61355832..61360280hg19UCSC Ensembl
Innerchr17:61355860..61360252hg19UCSC Ensembl
Outerchr17:61355804..61360308hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg384449
hg194449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv580e214
Supporting Variantsessv15720715
SamplesHG01841
Known GenesTANC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640987
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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