A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036560



Internal ID18779091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92870364..92918933hg38UCSC Ensembl
Innerchr15:93413594..93462163hg19UCSC Ensembl
Innerchr15:91214598..91263167hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3848570
hg1948570
hg1848570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2660n100
Supporting Variantsnssv3555232
Samples
Known GenesCHD2, LOC100507217, MIR3175
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036560
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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