A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066506



Internal ID19155725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75764481..75819490hg38UCSC Ensembl
Innerchr16:75798379..75853388hg19UCSC Ensembl
Innerchr16:74355880..74410889hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3855010
hg1955010
hg1855010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559629
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)nsv1066506
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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