A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074152



Internal ID15580652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143609267..143684812hg38UCSC Ensembl
Innerchr6:143930404..144005949hg19UCSC Ensembl
Innerchr6:143972097..144047642hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3875546
hg1975546
hg1875546
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604805
Supporting Variants
Samples
Known GenesPHACTR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1074152
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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