A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8809430



Internal ID13652072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157449642..157758815hg38UCSC Ensembl
Innerchr7:157451632..157757235hg38UCSC Ensembl
Outerchr7:157449532..157758935hg38UCSC Ensembl
chr7:157242336..157551507hg19UCSC Ensembl
Innerchr7:157244326..157549927hg19UCSC Ensembl
Outerchr7:157242226..157551627hg19UCSC Ensembl
chr7:156935097..157244268hg18UCSC Ensembl
Innerchr7:156937087..157242688hg18UCSC Ensembl
Outerchr7:156934987..157244388hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38309174
hg19309172
hg18309172
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3377143
Supporting Variants
SamplesNA12878
Known GenesMIR153-2, PTPRN2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8809430
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer