A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639642



Internal ID7026420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:792830..955116hg38UCSC Ensembl
chr17:696070..858356hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38162287
hg19162287
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15573152, essv15573151, essv15573153
SamplesNA11918, NA20318, NA18978
Known GenesNXN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639642
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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