A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1542037



Internal ID12358472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42534281..42534349hg38UCSC Ensembl
chr5:42534383..42534451hg19UCSC Ensembl
chr5:42570140..42570208hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3869
hg1969
hg1869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4328084
SamplesHuRef
Known GenesGHR
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1542037
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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