A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051957



Internal ID18794488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3417495..3444663hg38UCSC Ensembl
Innerchr16:3467495..3494663hg19UCSC Ensembl
Innerchr16:3407496..3434664hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3827169
hg1927169
hg1827169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556967
Samples
Known GenesNAA60, ZNF597
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051957
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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