A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559431



Internal ID18857712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64225597..64306468hg38UCSC Ensembl
Innerchr16:64259501..64340372hg19UCSC Ensembl
Innerchr16:62817002..62897873hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3880872
hg1980872
hg1880872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056675
Supporting Variants
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)nssv3559431
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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