A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759799



Internal ID18711394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103007876..103060114hg38UCSC Ensembl
Innerchr9:105770158..105822396hg19UCSC Ensembl
Innerchr9:104809979..104862217hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3852239
hg1952239
hg1852239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053646
Supporting Variants
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)nssv3759799
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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