A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040711



Internal ID19129930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76586021..76609916hg38UCSC Ensembl
Innerchr15:76878362..76902257hg19UCSC Ensembl
Innerchr15:74665417..74689312hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3823896
hg1923896
hg1823896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2629n100
Supporting Variantsnssv3554500, nssv3554499, nssv3554496, nssv3554498, nssv3554497
Samples
Known GenesSCAPER
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040711
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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