A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1045734



Internal ID15552234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177399337..177406217hg38UCSC Ensembl
Innerchr5:176826338..176833218hg19UCSC Ensembl
Innerchr5:176758944..176765824hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg386881
hg196881
hg186881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600368
Supporting Variants
Samples
Known GenesF12, PFN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1045734
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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