A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3570513



Internal ID6695209
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 StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992213
Supporting Variants
SamplesHuRef
Known GenesAFP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3570513
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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