A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035389



Internal ID19124608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76152354..76191001hg38UCSC Ensembl
Innerchr15:76444695..76483342hg19UCSC Ensembl
Innerchr15:74231750..74270397hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3838648
hg1938648
hg1838648
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2624n100
Supporting Variantsnssv3553716, nssv3553717, nssv3553715
Samples
Known GenesC15orf27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035389
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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