A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640507



Internal ID6680594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37781367..37854236hg38UCSC Ensembl
chr17:36141337..36213855hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3872870
hg1972519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15669528, essv15669529
SamplesNA20359, NA20362
Known GenesYWHAEP7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640507
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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