A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4198906



Internal ID11134758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114292010..114292010hg38UCSC Ensembl
chr7:113932065..113932065hg19UCSC Ensembl
chr7:113719301..113719301hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38231
hg19231
hg18231
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1301656
Supporting Variants
SamplesHuRef
Known GenesFOXP2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4198906
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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