A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786987



Internal ID19171199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:48039242..48099144hg38UCSC Ensembl
Innerchr3:48080732..48140634hg19UCSC Ensembl
Innerchr3:48055736..48115638hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3859903
hg1959903
hg1859903
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893693
Supporting Variants
Samples
Known GenesMAP4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786987
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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