A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605516



Internal ID16392925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169723586..169724924hg38UCSC Ensembl
Innerchr6:170123682..170125020hg19UCSC Ensembl
Innerchr6:169865607..169866945hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381339
hg191339
hg181339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11079n54
Supporting Variantsnssv1077372, nssv1077371
Samples
Known GenesPHF10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605516
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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