A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557851



Internal ID16345260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:27779963..27780856hg38UCSC Ensembl
Innerchr12:27932896..27933789hg19UCSC Ensembl
Innerchr12:27824163..27825056hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38894
hg19894
hg18894
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2425n54
Supporting Variantsnssv790070, nssv790069
Samples
Known GenesKLHL42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557851
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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