A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992213



Internal ID6728175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73446595..73446658hg38UCSC Ensembl
chr4:74312312..74312375hg19UCSC Ensembl
chr4:74531176..74531239hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3864
hg1964
hg1864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3570513
SamplesHuRef
Known GenesAFP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992213
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer