A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589770



Internal ID16377179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14264614..14312781hg38UCSC Ensembl
Innerchr3:14306114..14354281hg19UCSC Ensembl
Innerchr3:14281118..14329285hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3848168
hg1948168
hg1848168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959439
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589770
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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