A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639618



Internal ID7026397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:316193..343916hg38UCSC Ensembl
chr17:165984..193707hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3827724
hg1927724
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15570212
SamplesHG01935
Known GenesLOC100506388, RPH3AL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639618
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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