A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15578150



Internal ID2824779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:915092..924475hg38UCSC Ensembl
Innerchr17:915592..923975hg38UCSC Ensembl
Outerchr17:914092..925475hg38UCSC Ensembl
chr17:818332..827715hg19UCSC Ensembl
Innerchr17:818832..827215hg19UCSC Ensembl
Outerchr17:817332..828715hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg389384
hg199384
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639654
Supporting Variants
SamplesHG02493
Known GenesNXN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15578150
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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