A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035773



Internal ID18778304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:17040139..17263600hg38UCSC Ensembl
Innerchr16:17133996..17357457hg19UCSC Ensembl
Innerchr16:17041497..17264958hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38223462
hg19223462
hg18223462
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3716918
Samples
Known GenesXYLT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035773
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer