A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042909



Internal ID19132128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19934565..19959156hg38UCSC Ensembl
Innerchr16:19945887..19970478hg19UCSC Ensembl
Innerchr16:19853388..19877979hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3824592
hg1924592
hg1824592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2791n100
Supporting Variantsnssv3547004, nssv3547005
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)nsv1042909
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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