A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604841



Internal ID16045564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:147511020..147872793hg38UCSC Ensembl
Innerchr6:147832156..148193929hg19UCSC Ensembl
Innerchr6:147873849..148235622hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38361774
hg19361774
hg18361774
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1074347
Samples
Known GenesSAMD5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604841
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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