A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557835



Internal ID16345244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:27779899..27780856hg38UCSC Ensembl
Innerchr12:27932832..27933789hg19UCSC Ensembl
Innerchr12:27824099..27825056hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38958
hg19958
hg18958
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2425n54
Supporting Variantsnssv789990, nssv789991, nssv789989, nssv789988, nssv789987
Samples
Known GenesKLHL42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557835
Frequency
Sample Size17421
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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