A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641407



Internal ID6681492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81858294..81890680hg38UCSC Ensembl
chr17:79816170..79848556hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3832387
hg1932387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15764809, essv15764807, essv15764808
SamplesHG00451, NA12872, HG01951
Known GenesALYREF, ARHGDIA, P4HB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641407
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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