A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639617



Internal ID7026396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:307633..357098hg38UCSC Ensembl
chr17:157424..206889hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3849466
hg1949466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15570210, essv15570211, essv15570209
SamplesNA19461, NA19467, HG01935
Known GenesLOC100506388, RPH3AL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639617
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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