A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641217



Internal ID6681302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73333603..73354776hg38UCSC Ensembl
chr17:71329742..71350915hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3821174
hg1921174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15736086
SamplesNA19323
Known GenesSDK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641217
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer