A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691567



Internal ID18989848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:132786673..132848954hg38UCSC Ensembl
Innerchr8:133798919..133861199hg19UCSC Ensembl
Innerchr8:133868101..133930381hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3862282
hg1962281
hg1862281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034433
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)nssv3691567
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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