A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055636



Internal ID19144855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32169453..33970586hg38UCSC Ensembl
Innerchr16:32180774..33773053hg19UCSC Ensembl
Innerchr16:32088275..33680554hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381801134
hg191592280
hg181592280
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2844n100
Supporting Variantsnssv3716311, nssv3550390, nssv3716306, nssv3716305, nssv3716317, nssv3716314, nssv3716315, nssv3716313, nssv3550389, nssv3716309, nssv3716310, nssv3716308, nssv3550388, nssv3716312, nssv3716316, nssv3716307, nssv3716318
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055636
Frequency
Sample Size11257
Observed Gain16
Observed Loss1
Observed Complex0
Frequencyn/a


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