A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7472642



Internal ID10750924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88561995..88562044hg38UCSC Ensembl
chr16:88628403..88628452hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3203075
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7472642
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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