A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv798826



Internal ID16092782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73711173..73719248hg38UCSC Ensembl
Innerchr12:74104953..74113028hg19UCSC Ensembl
Innerchr12:72391220..72399295hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg388076
hg198076
hg188076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559387
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)nssv798826
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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