A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994957



Internal ID6730907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:105767533..105783119hg38UCSC Ensembl
Outerchr2:106383990..106399576hg19UCSC Ensembl
Outerchr2:105750422..105766008hg18UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg3815587
hg1915587
hg1815587
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565017
SamplesHuRef
Known GenesNCK2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994957
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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