A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691557



Internal ID18989838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:132783362..132833133hg38UCSC Ensembl
Innerchr8:133795608..133845378hg19UCSC Ensembl
Innerchr8:133864790..133914560hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3849772
hg1949771
hg1849771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019269
Supporting Variants
Samples
Known GenesPHF20L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691557
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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