A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639647



Internal ID7026425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:840725..872651hg38UCSC Ensembl
chr17:743965..775891hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3831927
hg1931927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15575932, essv15575931, essv15575929, essv15575928, essv15575930
SamplesNA20317, NA11918, NA20318, NA18978, HG01577
Known GenesNXN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639647
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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