A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675951



Internal ID18974232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16092468..16167255hg38UCSC Ensembl
Innerchr8:15949977..16024764hg19UCSC Ensembl
Innerchr8:15994348..16069135hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3874788
hg1974788
hg1874788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016636
Supporting Variants
Samples
Known GenesMSR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3675951
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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