A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639904



Internal ID7026682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9403722..9422199hg38UCSC Ensembl
Innerchr17:9403768..9422153hg38UCSC Ensembl
Outerchr17:9403676..9422245hg38UCSC Ensembl
chr17:9307039..9325516hg19UCSC Ensembl
Innerchr17:9307085..9325470hg19UCSC Ensembl
Outerchr17:9306993..9325562hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3818478
hg1918478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15610243
SamplesHG01765
Known GenesSTX8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639904
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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