A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077382



Internal ID15930568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169723871..169724975hg38UCSC Ensembl
Innerchr6:170123967..170125071hg19UCSC Ensembl
Innerchr6:169865892..169866996hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381105
hg191105
hg181105
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605525
Supporting Variants
Samples
Known GenesPHF10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1077382
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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