A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044772



Internal ID19133991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12554409..12574894hg38UCSC Ensembl
Innerchr16:12648266..12668751hg19UCSC Ensembl
Innerchr16:12555767..12576252hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3820486
hg1920486
hg1820486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2732n100
Supporting Variantsnssv3557162
Samples
Known GenesSNX29
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044772
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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