A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893713



Internal ID19184533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61613054..61687678hg38UCSC Ensembl
Outerchr3:61613054..61687678hg38UCSC Ensembl
Innerchr3:61598728..61673352hg19UCSC Ensembl
Outerchr3:61598728..61673352hg19UCSC Ensembl
Innerchr3:61573768..61648392hg18UCSC Ensembl
Outerchr3:61573768..61648392hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3874625
hg1974625
hg1874625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784999
Samples
Known GenesPTPRG
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893713
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer