A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997809



Internal ID18810659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4107112..4252986hg38UCSC Ensembl
Innerchr3:4148796..4294670hg19UCSC Ensembl
Innerchr3:4123796..4269670hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38145875
hg19145875
hg18145875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4652n100
Supporting Variantsnssv3590470
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)nsv997809
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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