A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1032914



Internal ID11849354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73446656..73446720hg38UCSC Ensembl
chr4:74312373..74312437hg19UCSC Ensembl
chr4:74531237..74531301hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3865
hg1965
hg1865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4218054
SamplesHuRef
Known GenesAFP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1032914
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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