A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013393



Internal ID18755924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164998562..165035342hg38UCSC Ensembl
Innerchr3:164716350..164753130hg19UCSC Ensembl
Innerchr3:166199044..166235824hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3836781
hg1936781
hg1836781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614545
Samples
Known GenesSI
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013393
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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