A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055510



Internal ID18798041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32069540..32453200hg38UCSC Ensembl
Innerchr16:32080861..32464521hg19UCSC Ensembl
Innerchr16:31988362..32372022hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38383661
hg19383661
hg18383661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2835n100
Supporting Variantsnssv3549328
Samples
Known GenesHERC2P4, LOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055510
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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