A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1767604



Internal ID12930722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91441918..91447699hg38UCSC Ensembl
chr10:93201675..93207456hg19UCSC Ensembl
chr10:93191655..93197436hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg385782
hg195782
hg185782
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3836360
SamplesHuRef
Known GenesHECTD2, LOC100188947
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1767604
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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