A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639614



Internal ID7026393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:176972..217320hg38UCSC Ensembl
chr17:26763..67111hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3840349
hg1940349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15570157
SamplesHG01935
Known GenesDOC2B, LOC100506371, RPH3AL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639614
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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