A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036917



Internal ID18779448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32992500..33020161hg38UCSC Ensembl
Innerchr15:33284701..33312362hg19UCSC Ensembl
Innerchr15:31071993..31099654hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3827662
hg1927662
hg1827662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2549n100
Supporting Variantsnssv3547871
Samples
Known GenesFMN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036917
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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