A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047585



Internal ID18790116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93942818..94435921hg38UCSC Ensembl
Innerchr15:94486047..94979150hg19UCSC Ensembl
Innerchr15:92287051..92780154hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38493104
hg19493104
hg18493104
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555266
Samples
Known GenesMCTP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047585
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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