A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3549332



Internal ID18847613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32069540..32624316hg38UCSC Ensembl
Innerchr16:32080861..32635637hg19UCSC Ensembl
Innerchr16:31988362..32543138hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38554777
hg19554777
hg18554777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064761
Supporting Variants
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)nssv3549332
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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