A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063509



Internal ID19152728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75921526..75995551hg38UCSC Ensembl
Innerchr16:75955424..76029449hg19UCSC Ensembl
Innerchr16:74512925..74586950hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3874026
hg1974026
hg1874026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3022n100
Supporting Variantsnssv3559635
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)nsv1063509
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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