A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675949



Internal ID18974230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16092468..16166875hg38UCSC Ensembl
Innerchr8:15949977..16024384hg19UCSC Ensembl
Innerchr8:15994348..16068755hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3874408
hg1974408
hg1874408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022644
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)nssv3675949
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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