A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997449



Internal ID19156985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104369700..104551178hg38UCSC Ensembl
Innerchr3:104088544..104270022hg19UCSC Ensembl
Innerchr3:105571234..105752712hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38181479
hg19181479
hg18181479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4832n100
Supporting Variantsnssv3735242
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)nsv997449
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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