A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4347347



Internal ID11629885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105908638..105908638hg38UCSC Ensembl
chr7:105549084..105549084hg19UCSC Ensembl
chr7:105336320..105336320hg18UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg38462
hg19462
hg18462
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1641219
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4347347
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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