A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613612



Internal ID16054335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12628213..12712157hg38UCSC Ensembl
Innerchr9:12628213..12712157hg19UCSC Ensembl
Innerchr9:12618213..12702157hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3883945
hg1983945
hg1883945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12568n54
Supporting Variantsnssv1128715
Samples
Known GenesTYRP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613612
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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