A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578716



Internal ID16366125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14978361..15002966hg38UCSC Ensembl
Innerchr19:15089173..15113778hg19UCSC Ensembl
Innerchr19:14950173..14974778hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3824606
hg1924606
hg1824606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv895572
Samples
Known GenesSLC1A6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578716
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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