A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557269



Internal ID15997992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7471128..7538538hg38UCSC Ensembl
Innerchr12:7623724..7691134hg19UCSC Ensembl
Innerchr12:7514991..7582401hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3867411
hg1967411
hg1867411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv787266
Samples
Known GenesCD163
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557269
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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