A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058920



Internal ID19148139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58351479..58387412hg38UCSC Ensembl
Innerchr16:58385383..58421316hg19UCSC Ensembl
Innerchr16:56942884..56978817hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3835934
hg1935934
hg1835934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2990n100
Supporting Variantsnssv3559359, nssv3559358, nssv3559357, nssv3559361, nssv3559360
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058920
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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