A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997027



Internal ID6732969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:17535283..17550583hg38UCSC Ensembl
Outerchr1:17861778..17877078hg19UCSC Ensembl
Outerchr1:17734365..17749665hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3815301
hg1915301
hg1815301
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564910
SamplesHuRef
Known GenesARHGEF10L
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997027
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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