A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557093



Internal ID18855374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7862523..7929135hg38UCSC Ensembl
Innerchr16:7912525..7979137hg19UCSC Ensembl
Innerchr16:7852526..7919138hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3866613
hg1966613
hg1866613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036899
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)nssv3557093
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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