A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037980



Internal ID18780511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68061238..68145365hg38UCSC Ensembl
Innerchr15:68353576..68437703hg19UCSC Ensembl
Innerchr15:66140630..66224757hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3884128
hg1984128
hg1884128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553654
Samples
Known GenesPIAS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037980
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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