A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv804215



Internal ID16098171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:128177571..128203476hg38UCSC Ensembl
Innerchr12:128662116..128688021hg19UCSC Ensembl
Innerchr12:127228069..127253974hg18UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3825906
hg1925906
hg1825906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560638
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv804215
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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