A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891694



Internal ID18839404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96278219..96369762hg38UCSC Ensembl
Outerchr9:96278219..96369762hg38UCSC Ensembl
Innerchr9:99040501..99132044hg19UCSC Ensembl
Outerchr9:99040501..99132044hg19UCSC Ensembl
Innerchr9:98080322..98171865hg18UCSC Ensembl
Outerchr9:98080322..98171865hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3891544
hg1991544
hg1891544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784165
Samples
Known GenesHSD17B3, SLC35D2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891694
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