A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12755682



Internal ID2302614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42733273..42739374hg38UCSC Ensembl
Innerchr7:42733405..42739242hg38UCSC Ensembl
Outerchr7:42733141..42739506hg38UCSC Ensembl
chr7:42772872..42778973hg19UCSC Ensembl
Innerchr7:42773004..42778841hg19UCSC Ensembl
Outerchr7:42772740..42779105hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg386102
hg196102
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612975
Supporting Variants
SamplesHG02053
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12755682
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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