A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718094



Internal ID19016375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77292033..77384615hg38UCSC Ensembl
Innerchr15:77584375..77676957hg19UCSC Ensembl
Innerchr15:75371430..75464012hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3892583
hg1992583
hg1892583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040430
Supporting Variants
Samples
Known GenesPEAK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718094
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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