A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1437076



Internal ID12600198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112139697..112139751hg38UCSC Ensembl
chr2:112897274..112897328hg19UCSC Ensembl
chr2:112613745..112613799hg18UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3855
hg1955
hg1855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3655270
SamplesHuRef
Known GenesFBLN7
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1437076
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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