A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015671



Internal ID19104889
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 StatusM
Merged Variantsdgv5919n100
Supporting Variantsnssv3749033
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)nsv1015671
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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