A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019469



Internal ID19108687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73934492..73992700hg38UCSC Ensembl
Innerchr6:74644208..74702416hg19UCSC Ensembl
Innerchr6:74700936..74759136hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3858209
hg1958209
hg1858201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747084
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)nsv1019469
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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