A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784165



Internal ID18833419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96278219..96369762hg38UCSC Ensembl
Innerchr9:99040501..99132044hg19UCSC Ensembl
Innerchr9:98080322..98171865hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3891544
hg1991544
hg1891544
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891694
Supporting Variants
Samples
Known GenesHSD17B3, SLC35D2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=28
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784165
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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