A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891732



Internal ID19186128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136725859..136806153hg38UCSC Ensembl
Outerchr9:136725859..136806153hg38UCSC Ensembl
Innerchr9:139620311..139700605hg19UCSC Ensembl
Outerchr9:139620311..139700605hg19UCSC Ensembl
Innerchr9:138740132..138820426hg18UCSC Ensembl
Outerchr9:138740132..138820426hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3880295
hg1980295
hg1880295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778432
Samples
Known GenesCCDC183, CCDC183-AS1, LCN10, LCN15, LCN6, LCN8, LOC100128593, MIR6722, SNHG7, SNORA17, SNORA43, TMEM141
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891732
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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