A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037456



Internal ID18779987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10765..65187hg38UCSC Ensembl
Innerchr16:60765..115185hg19UCSC Ensembl
Innerchr16:765..55185hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3854423
hg1954421
hg1854421
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718826, nssv3556929
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)nsv1037456
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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