A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892081



Internal ID18839791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13472989..13621730hg38UCSC Ensembl
Outerchr1:13472989..13621730hg38UCSC Ensembl
Innerchr1:13799457..13948225hg19UCSC Ensembl
Outerchr1:13799457..13948225hg19UCSC Ensembl
Innerchr1:13672044..13820812hg18UCSC Ensembl
Outerchr1:13672044..13820812hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38148742
hg19148769
hg18148769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785248
Samples
Known GenesLRRC38, PDPN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892081
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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