A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999089



Internal ID19158625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:165549232..165591068hg38UCSC Ensembl
Innerchr3:165267020..165308856hg19UCSC Ensembl
Innerchr3:166749714..166791550hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3841837
hg1941837
hg1841837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4974n100
Supporting Variantsnssv3612659
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999089
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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