A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3552319



Internal ID18503914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43600874..43703678hg38UCSC Ensembl
Innerchr15:43893072..43995876hg19UCSC Ensembl
Innerchr15:41680364..41783168hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38102805
hg19102805
hg18102805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049269
Supporting Variants
Samples
Known GenesCATSPER2, CKMT1A, RNU6-28P, STRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3552319
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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