A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046192



Internal ID18788723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70930702..71121309hg38UCSC Ensembl
Innerchr15:71223041..71413648hg19UCSC Ensembl
Innerchr15:69010095..69200702hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38190608
hg19190608
hg18190608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717958
Samples
Known GenesCT62, LRRC49
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046192
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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