A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559371



Internal ID18857652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:62609649..62703267hg38UCSC Ensembl
Innerchr16:62643553..62737171hg19UCSC Ensembl
Innerchr16:61201054..61294672hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3893619
hg1993619
hg1893619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057167
Supporting Variants
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)nssv3559371
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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