A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077364



Internal ID15930550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169722138..169724975hg38UCSC Ensembl
Innerchr6:170122234..170125071hg19UCSC Ensembl
Innerchr6:169864159..169866996hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382838
hg192838
hg182838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605509
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)nssv1077364
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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