A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060082



Internal ID19149301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:61220255..61466456hg38UCSC Ensembl
Innerchr16:61254159..61500360hg19UCSC Ensembl
Innerchr16:59811660..60057861hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38246202
hg19246202
hg18246202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722720
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)nsv1060082
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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