A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7532396



Internal ID10463992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:48709126..48709449hg38UCSC Ensembl
Outerchr10:49917171..49917494hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3262829
Supporting Variants
SamplesHuRef
Known GenesWDFY4
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7532396
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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