A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15664523



Internal ID6694156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35353788..35442365hg38UCSC Ensembl
chr17:33680807..33769384hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3888578
hg1988578
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640449
Supporting Variants
SamplesNA20821
Known GenesSLFN11, SLFN12, SLFN13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15664523
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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