A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648896



Internal ID18947177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85764650..85837362hg38UCSC Ensembl
Innerchr6:86474368..86547080hg19UCSC Ensembl
Innerchr6:86531087..86603799hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3872713
hg1972713
hg1872713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031231
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3648896
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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