A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044188



Internal ID19133407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19934799..19959156hg38UCSC Ensembl
Innerchr16:19946121..19970478hg19UCSC Ensembl
Innerchr16:19853622..19877979hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3824358
hg1924358
hg1824358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2791n100
Supporting Variantsnssv3547029, nssv3547030, nssv3547031
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)nsv1044188
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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