A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15666458



Internal ID5668274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36602406..36633068hg38UCSC Ensembl
chr17:34958835..34989526hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3830663
hg1930692
Variant TypeCNV gain
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640475
Supporting Variants
SamplesNA20359
Known GenesMRM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15666458
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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