A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778981



Internal ID19175912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75505538..75538114hg38UCSC Ensembl
Innerchr16:75539436..75572012hg19UCSC Ensembl
Innerchr16:74096937..74129513hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3832577
hg1932577
hg1832577
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892888
Supporting Variants
Samples
Known GenesCHST5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778981
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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