A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175875



Internal ID15854418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:74464177..74528943hg38UCSC Ensembl
Innerchr12:74857957..74922723hg19UCSC Ensembl
Innerchr12:73144224..73208990hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3864767
hg1964767
hg1864767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559416
Supporting Variants
Samples1780862109_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175875
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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