A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602751



Internal ID16390160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32644620..32656837hg38UCSC Ensembl
Innerchr6:32612397..32624614hg19UCSC Ensembl
Innerchr6:32720375..32732592hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3812218
hg1912218
hg1812218
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10593n54
Supporting Variantsnssv1056641, nssv1056648, nssv1056651, nssv1056650, nssv1056647, nssv1056646, nssv1056644, nssv1056643, nssv1056642, nssv1056649, nssv1056645
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602751
Frequency
Sample Size17421
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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