A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001179



Internal ID19090396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37935209..37945639hg38UCSC Ensembl
Innerchr3:37976700..37987130hg19UCSC Ensembl
Innerchr3:37951704..37962134hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3810431
hg1910431
hg1810431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4721n100
Supporting Variantsnssv3589690
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001179
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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