A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv802670



Internal ID16096626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:112574591..112587857hg38UCSC Ensembl
Innerchr12:113012395..113025661hg19UCSC Ensembl
Innerchr12:111496778..111510044hg18UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3813267
hg1913267
hg1813267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560257
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)nssv802670
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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