A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052935



Internal ID19142154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20522307..20594995hg38UCSC Ensembl
Innerchr16:20533629..20606317hg19UCSC Ensembl
Innerchr16:20441130..20513818hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3872689
hg1972689
hg1872689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3548038
Samples
Known GenesACSM2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052935
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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