A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005098



Internal ID6717221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134449369..134449369hg38UCSC Ensembl
chr6:134770507..134770507hg19UCSC Ensembl
chr6:134812200..134812200hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3860
hg1960
hg1860
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3578375
SamplesHuRef
Known GenesLINC01010
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005098
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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