A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640299



Internal ID6680386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27786758..27787312hg38UCSC Ensembl
Innerchr17:27786984..27787086hg38UCSC Ensembl
Outerchr17:27786532..27787538hg38UCSC Ensembl
chr17:26113784..26114338hg19UCSC Ensembl
Innerchr17:26114010..26114112hg19UCSC Ensembl
Outerchr17:26113558..26114564hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15655727
SamplesNA18916
Known GenesNOS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640299
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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