A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15731868



Internal ID3300255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69904807..69905318hg38UCSC Ensembl
Innerchr17:69904809..69905317hg38UCSC Ensembl
Outerchr17:69904806..69905320hg38UCSC Ensembl
chr17:67900948..67901459hg19UCSC Ensembl
Innerchr17:67900950..67901458hg19UCSC Ensembl
Outerchr17:67900947..67901461hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641138
Supporting Variants
SamplesHG02943
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15731868
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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