A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv849046



Internal ID16143002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:95480265..95520420hg38UCSC Ensembl
Innerchr15:96023494..96063649hg19UCSC Ensembl
Innerchr15:93824498..93864653hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3840156
hg1940156
hg1840156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570564
Supporting Variants
Samples
Known GenesLINC00924
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv849046
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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