A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045580



Internal ID19134799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19934565..19956028hg38UCSC Ensembl
Innerchr16:19945887..19967350hg19UCSC Ensembl
Innerchr16:19853388..19874851hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3821464
hg1921464
hg1821464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2789n100
Supporting Variantsnssv3546997, nssv3547003, nssv3719261, nssv3547002, nssv3546998, nssv3546996, nssv3547001, nssv3546999, nssv3547000
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)nsv1045580
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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