A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15575946



Internal ID4786921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:886198..919987hg38UCSC Ensembl
chr17:789438..823227hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3833790
hg1933790
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639650
Supporting Variants
SamplesNA11918
Known GenesNXN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15575946
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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