A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056252



Internal ID19145471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79557382..79574934hg38UCSC Ensembl
Innerchr16:79591279..79608831hg19UCSC Ensembl
Innerchr16:78148780..78166332hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3817553
hg1917553
hg1817553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3041n100
Supporting Variantsnssv3559776
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)nsv1056252
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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