A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687477



Internal ID18985758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:50716059..50949590hg38UCSC Ensembl
Innerchr8:51628619..51862150hg19UCSC Ensembl
Innerchr8:51791172..52024703hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38233532
hg19233532
hg18233532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019760
Supporting Variants
Samples
Known GenesSNTG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3687477
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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