A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749033



Internal ID19047314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:15026899..15062921hg38UCSC Ensembl
Innerchr6:15027130..15063152hg19UCSC Ensembl
Innerchr6:15135109..15171131hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3836023
hg1936023
hg1836023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015671
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)nssv3749033
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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