A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043424



Internal ID18785955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102981556..103000775hg38UCSC Ensembl
Innerchr9:105743838..105763057hg19UCSC Ensembl
Innerchr9:104783659..104802878hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3819220
hg1919220
hg1819220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697601
Samples
Known GenesCYLC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043424
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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