A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999990



Internal ID19159526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:25875675..25922093hg38UCSC Ensembl
Innerchr3:25917166..25963584hg19UCSC Ensembl
Innerchr3:25892170..25938588hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3846419
hg1946419
hg1846419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589516
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)nsv999990
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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