A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061104



Internal ID19150323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32069540..33970586hg38UCSC Ensembl
Innerchr16:32080861..33773053hg19UCSC Ensembl
Innerchr16:31988362..33680554hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381901047
hg191692193
hg181692193
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2844n100
Supporting Variantsnssv3549367, nssv3549368, nssv3549365, nssv3549366, nssv3716247, nssv3549371, nssv3549364, nssv3549370, nssv3549369
Samples
Known GenesHERC2P4, LOC390705, 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)nsv1061104
Frequency
Sample Size11257
Observed Gain8
Observed Loss1
Observed Complex0
Frequencyn/a


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