A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639641



Internal ID7026419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:776211..827076hg38UCSC Ensembl
chr17:679451..730316hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3850866
hg1950866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15573150, essv15573148, essv15573149
SamplesNA20317, NA20318, NA18978
Known GenesGLOD4, NXN, RNMTL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639641
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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