A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043694



Internal ID19132913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10765..69731hg38UCSC Ensembl
Innerchr16:60765..119729hg19UCSC Ensembl
Innerchr16:765..59729hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3858967
hg1958965
hg1858965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2688n100
Supporting Variantsnssv3556930, nssv3556931
Samples
Known GenesDDX11L10, LOC100288778, MIR6859-1, MIR6859-2, POLR3K, RHBDF1, SNRNP25
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043694
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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