A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799962



Internal ID19173165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5297563..5355536hg38UCSC Ensembl
Innerchr9:5297563..5355536hg19UCSC Ensembl
Innerchr9:5287563..5345536hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3857974
hg1957974
hg1857974
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891539
Supporting Variants
Samples
Known GenesRLN1, RLN2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799962
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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