A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639658



Internal ID7026436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:924351..925517hg38UCSC Ensembl
Innerchr17:924351..925517hg38UCSC Ensembl
Outerchr17:924036..925787hg38UCSC Ensembl
chr17:827591..828757hg19UCSC Ensembl
Innerchr17:827591..828757hg19UCSC Ensembl
Outerchr17:827276..829027hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381167
hg191167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15578157
SamplesHG00671
Known GenesNXN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639658
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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