A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039024



Internal ID18781555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103000721..103050888hg38UCSC Ensembl
Innerchr9:105763003..105813170hg19UCSC Ensembl
Innerchr9:104802824..104852991hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3850168
hg1950168
hg1850168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7693n100
Supporting Variantsnssv3697602
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)nsv1039024
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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