A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639898



Internal ID7026676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9300046..9303144hg38UCSC Ensembl
Innerchr17:9300546..9302644hg38UCSC Ensembl
Outerchr17:9299046..9304144hg38UCSC Ensembl
chr17:9203363..9206461hg19UCSC Ensembl
Innerchr17:9203863..9205961hg19UCSC Ensembl
Outerchr17:9202363..9207461hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg383099
hg193099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15610234
SamplesHG00335
Known GenesSTX8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639898
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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