A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1111214



Internal ID15964400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39451651..39499982hg38UCSC Ensembl
Innerchr8:39309170..39357501hg19UCSC Ensembl
Innerchr8:39428327..39476658hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3848332
hg1948332
hg1848332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611057
Supporting Variants
Samples
Known GenesADAM3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1111214
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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