A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010735



Internal ID6722826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88760320..88760641hg38UCSC Ensembl
chr4:89681471..89681792hg19UCSC Ensembl
chr4:89900494..89900815hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38322
hg19322
hg18322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3583142
SamplesHuRef
Known GenesFAM13A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010735
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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