A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602868



Internal ID16390277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34236065..34238257hg38UCSC Ensembl
Innerchr6:34203842..34206034hg19UCSC Ensembl
Innerchr6:34311820..34314012hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg382193
hg192193
hg182193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10616n54
Supporting Variantsnssv1057878
Samples
Known GenesHMGA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602868
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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