A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4092286



Internal ID11322903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70409105..70409105hg38UCSC Ensembl
chr9:73024021..73024021hg19UCSC Ensembl
chr9:72213841..72213841hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3866
hg1966
hg1866
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1491500
Supporting Variants
SamplesHuRef
Known GenesKLF9
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4092286
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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