A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4270452



Internal ID11206304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2553995..2567688hg38UCSC Ensembl
chr1:2485434..2499127hg19UCSC Ensembl
chr1:2475133..2489144hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3813694
hg1913694
hg1814012
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1699286
Supporting Variants
SamplesHuRef
Known GenesLOC100133445, TNFRSF14
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4270452
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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