A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1301656



Internal ID12118092
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4198906
SamplesHuRef
Known GenesFOXP2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1301656
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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