A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1682998



Internal ID12846116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143819344..144265149hg38UCSC Ensembl
chr7:143516437..143962242hg19UCSC Ensembl
chr7:143147370..143593175hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38445806
hg19445806
hg18445806
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3855395
SamplesHuRef
Known GenesARHGEF34P, ARHGEF35, CTAGE4, FAM115A, LOC154761, OR2A1, OR2A12, OR2A14, OR2A2, OR2A20P, OR2A25, OR2A42, OR2A5, OR2A7, OR2A9P, OR2F1, OR2F2, OR6B1, RNU6-57P
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1682998
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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