A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687468



Internal ID18639063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:49304706..51268573hg38UCSC Ensembl
Innerchr8:50217265..52181133hg19UCSC Ensembl
Innerchr8:50379818..52343686hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg381963868
hg191963869
hg181963869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031818
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)nssv3687468
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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