A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1398337



Internal ID12561459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75022481..75022481hg38UCSC Ensembl
chr7:74436649..74436649hg19UCSC Ensembl
chr7:74074585..74074585hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3857
hg1957
hg1857
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4042681
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1398337
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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