A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045842



Internal ID19135061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20453186..20489701hg38UCSC Ensembl
Innerchr16:20464508..20501023hg19UCSC Ensembl
Innerchr16:20372009..20408524hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3836516
hg1936516
hg1836516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2796n100
Supporting Variantsnssv3547117
Samples
Known GenesACSM2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045842
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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