A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077363



Internal ID15583863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169719393..169724975hg38UCSC Ensembl
Innerchr6:170119489..170125071hg19UCSC Ensembl
Innerchr6:169861414..169866996hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg385583
hg195583
hg185583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605508
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)nssv1077363
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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