A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15753387



Internal ID5755203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79692179..79707682hg38UCSC Ensembl
Innerchr17:79692193..79707668hg38UCSC Ensembl
Outerchr17:79692165..79707696hg38UCSC Ensembl
chr17:77666109..77681491hg19UCSC Ensembl
Innerchr17:77666123..77681477hg19UCSC Ensembl
Outerchr17:77666095..77681505hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3815504
hg1915383
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641354
Supporting Variants
SamplesHG02733
Known GenesMIR4739
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15753387
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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