A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056863



Internal ID18799394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70015881..70091259hg38UCSC Ensembl
Innerchr16:70049784..70125162hg19UCSC Ensembl
Innerchr16:68607285..68682663hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3875379
hg1975379
hg1875379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559490
Samples
Known GenesMIR1972-1, MIR1972-2, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056863
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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