A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062253



Internal ID19151472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33970586..34161490hg38UCSC Ensembl
Innerchr16:33773053..33963957hg19UCSC Ensembl
Innerchr16:33680554..33871458hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38190905
hg19190905
hg18190905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2958n100
Supporting Variantsnssv3555953
Samples
Known GenesLINC00273
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062253
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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