A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784999



Internal ID19171435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61613054..61687678hg38UCSC Ensembl
Innerchr3:61598728..61673352hg19UCSC Ensembl
Innerchr3:61573768..61648392hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3874625
hg1974625
hg1874625
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893713
Supporting Variants
Samples
Known GenesPTPRG
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=28
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784999
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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