A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718214



Internal ID19016495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:95480714..95521087hg38UCSC Ensembl
Innerchr15:96023943..96064316hg19UCSC Ensembl
Innerchr15:93824947..93865320hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3840374
hg1940374
hg1840374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035312
Supporting Variants
Samples
Known GenesLINC00924
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718214
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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