A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052648



Internal ID18795179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15009807..15434384hg38UCSC Ensembl
Innerchr16:15103664..15528241hg19UCSC Ensembl
Innerchr16:15011165..15435742hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38424578
hg19424578
hg18424578
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2755n100
Supporting Variantsnssv3718981
Samples
Known GenesMIR1972-1, MIR1972-2, MIR3180-4, MIR6511B-1, MPV17L, NPIPA5, NTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052648
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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