A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002361



Internal ID19091578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226041688..226086595hg38UCSC Ensembl
Innerchr2:226906404..226951311hg19UCSC Ensembl
Innerchr2:226614648..226659555hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3844908
hg1944908
hg1844908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586829
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)nsv1002361
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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