A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3855395



Internal ID11906476
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 StatusS
Merged Variantsesv1682998
Supporting Variants
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)essv3855395
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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