A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038235



Internal ID19127454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8442801..8492583hg38UCSC Ensembl
Innerchr16:8492803..8542585hg19UCSC Ensembl
Innerchr16:8432804..8482586hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3849783
hg1949783
hg1849783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557103
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)nsv1038235
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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