A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749715



Internal ID19047996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168787638..168822314hg38UCSC Ensembl
Innerchr6:169187733..169222409hg19UCSC Ensembl
Innerchr6:168929658..168964334hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3834677
hg1934677
hg1834677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021422
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)nssv3749715
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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