A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061650



Internal ID19150869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60018433..60057275hg38UCSC Ensembl
Innerchr16:60052337..60091179hg19UCSC Ensembl
Innerchr16:58609838..58648680hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3838843
hg1938843
hg1838843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559365
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)nsv1061650
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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