A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1096622



Internal ID12259747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129144665..129144665hg38UCSC Ensembl
chr7:128784719..128784719hg19UCSC Ensembl
chr7:128571955..128571955hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38214
hg19214
hg18214
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4208192
SamplesHuRef
Known GenesTSPAN33
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1096622
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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