A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639896



Internal ID6679986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9251947..9255267hg38UCSC Ensembl
Innerchr17:9251947..9255267hg38UCSC Ensembl
Outerchr17:9251797..9255429hg38UCSC Ensembl
chr17:9155264..9158584hg19UCSC Ensembl
Innerchr17:9155264..9158584hg19UCSC Ensembl
Outerchr17:9155114..9158746hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg383321
hg193321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15610217
SamplesHG02332
Known GenesSTX8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639896
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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